| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003331.4 | 3159 | Missense Mutation | GCG,TCG | A1016S | NP_003322.3 |
| XM_011528245.1 | 3159 | Missense Mutation | GCG,TCG | A1016S | XP_011526547.1 |
| XM_011528246.2 | 3159 | Missense Mutation | GCG,TCG | A917S | XP_011526548.1 |
| XM_011528247.1 | 3159 | Missense Mutation | GCG,TCG | A917S | XP_011526549.1 |
| XM_011528249.2 | 3159 | Missense Mutation | GCG,TCG | A574S | XP_011526551.1 |
| XM_011528251.1 | 3159 | Missense Mutation | GCG,TCG | A435S | XP_011526553.1 |
| XM_011528252.1 | 3159 | Intron | XP_011526554.1 |