Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199821.1 | 312 | Missense Mutation | GCG,GTG | A66V | NP_001186750.1 |
NM_001199822.1 | 312 | Missense Mutation | GCG,GTG | A66V | NP_001186751.1 |
NM_138476.3 | 312 | Missense Mutation | GCG,GTG | A66V | NP_612485.2 |