Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001207019.2 | 877 | Missense Mutation | CGT,GGT | R265G | NP_001193948.2 |
NM_001220500.1 | 877 | Missense Mutation | CGT,GGT | R266G | NP_001207429.1 |
NM_002002.4 | 877 | Missense Mutation | CGT,GGT | R266G | NP_001993.2 |
XM_005272462.4 | 877 | Missense Mutation | CGT,GGT | R266G | XP_005272519.1 |