Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317195.1 | 672 | Missense Mutation | GCG,GTG | A43V | NP_001304124.1 |
NM_001317196.1 | 672 | Intron | NP_001304125.1 | ||
NM_001793.5 | 672 | Missense Mutation | GCG,GTG | A43V | NP_001784.2 |
XM_011522800.2 | 672 | Missense Mutation | GCG,GTG | A43V | XP_011521102.1 |