Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000079.3 | 1322 | Missense Mutation | GCG,GTG | A415V | NP_000070.1 |
NM_001039523.2 | 1322 | Missense Mutation | GCG,GTG | A440V | NP_001034612.1 |
XM_017003256.1 | 1322 | Missense Mutation | GCG,GTG | A447V | XP_016858745.1 |
XM_017003257.1 | 1322 | Missense Mutation | GCG,GTG | A422V | XP_016858746.1 |