Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001105538.1 | 3738 | Missense Mutation | AGG,GGG | R1226G | NP_001099008.1 |
NM_014520.3 | 3738 | Missense Mutation | AGG,GGG | R1226G | NP_055335.2 |
XM_011523616.2 | 3738 | Missense Mutation | AGG,GGG | R974G | XP_011521918.1 |