| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143780.2 | 956 | Missense Mutation | GCG,GTG | A289V | NP_001137252.1 |
| NM_001321240.1 | 956 | Missense Mutation | GCG,GTG | A266V | NP_001308169.1 |
| NM_001321241.1 | 956 | Missense Mutation | GCG,GTG | A287V | NP_001308170.1 |
| NM_016016.3 | 956 | Missense Mutation | GCG,GTG | A281V | NP_057100.1 |
| XM_011524880.2 | 956 | Missense Mutation | GCG,GTG | A295V | XP_011523182.1 |
| XM_011524882.2 | 956 | Missense Mutation | GCG,GTG | A272V | XP_011523184.1 |
| XM_011524883.2 | 956 | Missense Mutation | GCG,GTG | A194V | XP_011523185.1 |
| XM_011524884.1 | 956 | Missense Mutation | GCG,GTG | A194V | XP_011523186.1 |
| XM_017024737.1 | 956 | Missense Mutation | GCG,GTG | A188V | XP_016880226.1 |