| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_144702.2 | 249 | Missense Mutation | GCG,GTG | A26V | NP_653303.2 |
| XM_005244926.3 | 249 | Missense Mutation | GCG,GTG | A26V | XP_005244983.1 |
| XM_005244927.3 | 249 | Missense Mutation | GCG,GTG | A26V | XP_005244984.1 |
| XM_005244928.2 | 249 | Missense Mutation | GCG,GTG | A26V | XP_005244985.1 |
| XM_006711185.3 | 249 | Intron | XP_006711248.1 | ||
| XM_006711186.3 | 249 | Missense Mutation | GCG,GTG | A26V | XP_006711249.1 |
| XM_006711187.3 | 249 | Missense Mutation | GCG,GTG | A26V | XP_006711250.1 |
| XM_011509239.2 | 249 | Intron | XP_011507541.1 | ||
| XM_011509240.2 | 249 | Intron | XP_011507542.1 | ||
| XM_011509241.2 | 249 | Missense Mutation | GCG,GTG | A26V | XP_011507543.1 |
| XM_017000459.1 | 249 | Missense Mutation | GCG,GTG | A26V | XP_016855948.1 |
| XM_017000460.1 | 249 | Intron | XP_016855949.1 | ||
| XM_017000461.1 | 249 | Intron | XP_016855950.1 | ||
| XM_017000462.1 | 249 | Intron | XP_016855951.1 |