THE CODON IS ATT-GAG-CAT-CAA-AAT-CCG 1. What is the amino acid strand
Ile-Glu-His-Gln-Asn-Pro Stop-Leu-Val-Leu-Gly Phe-Ser-Arg-Asn-Thr Stop-Cys-Tyr-Stop-Thr
2. What is the amino acid sequence of the following mutatation? (if there is an incomplete amino acid please just use -x) ATT-GAG-CAG-TCA-AAA-TCC-G type your answer..

THERE ARE TWO QUESTIONS PLZ HELP ​

1. Ile Leu Glu Gly Leu Sec His Ile Ser Gly Leu Asn Ala Ser Asn Pro Arg ⇥ Ser Thr ⇥ Pro Leu Glu Sec Val Ala Leu Leu Glu Sec Gly Leu Tyr Pro His Glu Ser Glu Arg Ala Arg Gly Ala Ser Asn Thr His Arg Ser Thr ⇥ Pro Cys Tyr Ser Thr Tyr Arg Ser Thr ⇥ Pro Thr His Arg

2. Ala Thr Thr Glu Gln Thr Gln Ala Ala Thr Pro

Explanation:

I hope its correct , sorry if it's not

blue stars have the highest surface temp

stellar distances are usually expressed in light-years

the measure of a star's brightness is called magnitude

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an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.