| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145138.1 | 1200 | Missense Mutation | GCT,GGT | A428G | NP_001138610.1 |
| NM_001243984.1 | 1200 | Missense Mutation | GCT,GGT | A362G | NP_001230913.1 |
| NM_001243985.1 | 1200 | Intron | NP_001230914.1 | ||
| NM_021975.3 | 1200 | Missense Mutation | GCT,GGT | A431G | NP_068810.3 |
| XM_011545206.1 | 1200 | Missense Mutation | GCT,GGT | A360G | XP_011543508.1 |
| XM_011545207.1 | 1200 | Missense Mutation | GCT,GGT | A325G | XP_011543509.1 |