| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318359.1 | 485 | Intron | NP_001305288.1 | ||
| NM_018177.5 | 485 | Intron | NP_060647.2 | ||
| XM_006714023.3 | 485 | Intron | XP_006714086.1 | ||
| XM_011513716.2 | 485 | Missense Mutation | GCG,GGG | A101G | XP_011512018.1 |
| XM_011513717.2 | 485 | Missense Mutation | GCG,GGG | A101G | XP_011512019.1 |
| XM_011513718.2 | 485 | Intron | XP_011512020.1 | ||
| XM_011513719.2 | 485 | Intron | XP_011512021.1 | ||
| XM_011513720.1 | 485 | Intron | XP_011512022.1 | ||
| XM_011513721.1 | 485 | Intron | XP_011512023.1 | ||
| XM_017008397.1 | 485 | Missense Mutation | GCG,GGG | A101G | XP_016863886.1 |
| XM_017008398.1 | 485 | Intron | XP_016863887.1 | ||
| XM_017008399.1 | 485 | Intron | XP_016863888.1 |