| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001131007.1 | 227 | Missense Mutation | GCG,GTG | A42V | NP_001124479.1 |
| NM_015196.3 | 227 | Missense Mutation | GCG,GTG | A42V | NP_056011.3 |
| XM_011531780.1 | 227 | Missense Mutation | GCG,GTG | A71V | XP_011530082.1 |
| XM_011531781.1 | 227 | Missense Mutation | GCG,GTG | A71V | XP_011530083.1 |
| XM_011531783.1 | 227 | Missense Mutation | GCG,GTG | A71V | XP_011530085.1 |
| XM_017007924.1 | 227 | Missense Mutation | GCG,GTG | A71V | XP_016863413.1 |
| XM_017007925.1 | 227 | Missense Mutation | GCG,GTG | A42V | XP_016863414.1 |
| XM_017007926.1 | 227 | Missense Mutation | GCG,GTG | A42V | XP_016863415.1 |
| XM_017007927.1 | 227 | Intron | XP_016863416.1 |