| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001201550.2 | 162 | Missense Mutation | GCG,GTG | A21V | NP_001188479.1 |
| NM_001201551.1 | 162 | Missense Mutation | GCG,GTG | A20V | NP_001188480.1 |
| NM_006684.4 | 162 | Missense Mutation | GCG,GTG | A21V | NP_006675.2 |
| XM_006711129.3 | 162 | Intron | XP_006711192.1 | ||
| XM_017000110.1 | 162 | Intron | XP_016855599.1 | ||
| XM_017000111.1 | 162 | Missense Mutation | GCG,GTG | A21V | XP_016855600.1 |
| XM_017000112.1 | 162 | Intron | XP_016855601.1 | ||
| XM_017000113.1 | 162 | Missense Mutation | GCG,GTG | A21V | XP_016855602.1 |
| XM_017000114.1 | 162 | Intron | XP_016855603.1 |