| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145159.2 | 1999 | Missense Mutation | GCG,GTG | A624V | NP_001138631.1 |
| NM_001172562.1 | 1999 | Missense Mutation | GCG,GTG | A621V | NP_001166033.1 |
| NM_018250.3 | 1999 | Missense Mutation | GCG,GTG | A645V | NP_060720.2 |
| XM_006716356.2 | 1999 | Missense Mutation | GCG,GTG | A663V | XP_006716419.1 |
| XM_006716357.3 | 1999 | Intron | XP_006716420.1 | ||
| XM_011544573.1 | 1999 | Missense Mutation | GCG,GTG | A642V | XP_011542875.1 |
| XM_011544574.1 | 1999 | Missense Mutation | GCG,GTG | A639V | XP_011542876.1 |
| XM_011544575.2 | 1999 | Missense Mutation | GCG,GTG | A639V | XP_011542877.1 |
| XM_011544576.1 | 1999 | Missense Mutation | GCG,GTG | A618V | XP_011542878.1 |