Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145536.1 | 618 | Missense Mutation | CCG,TCG | P170S | NP_001139008.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000080.3 | 618 | Intron | NP_000071.1 | ||
XM_017024115.1 | 618 | Intron | XP_016879604.1 |