| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145304.1 | 4196 | Missense Mutation | GCG,GTG | A1327V | NP_001138776.1 |
| NM_001145305.1 | 4196 | Missense Mutation | GCG,GTG | A1094V | NP_001138777.1 |
| NM_025249.3 | 4196 | Missense Mutation | GCG,GTG | A1140V | NP_079525.1 |
| XM_005260084.1 | 4196 | Missense Mutation | GCG,GTG | A1327V | XP_005260141.1 |
| XM_011528324.1 | 4196 | Missense Mutation | GCG,GTG | A1281V | XP_011526626.1 |