Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_199337.2 | 443 | Missense Mutation | GCC,GTC | A111V | NP_955369.1 |
XM_005273982.3 | 443 | Missense Mutation | GCC,GTC | A141V | XP_005274039.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080501.2 | 443 | Intron | NP_001073970.1 |