| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001288587.2 | 1192 | Missense Mutation | GCG,GTG | A88V | NP_001275516.1 |
| NM_001321630.1 | 1192 | Missense Mutation | GCG,GTG | A88V | NP_001308559.1 |
| NM_032899.6 | 1192 | Missense Mutation | GCG,GTG | A88V | NP_116288.2 |
| NM_207006.2 | 1192 | Missense Mutation | GCG,GTG | A88V | NP_996889.1 |
| XM_005251087.2 | 1192 | Missense Mutation | GCG,GTG | A88V | XP_005251144.1 |
| XM_011517338.1 | 1192 | Missense Mutation | GCG,GTG | A88V | XP_011515640.1 |