| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_138424.1 | 1467 | Missense Mutation | CGT,TGT | R330C | NP_612433.1 |
| XM_005251683.4 | 1467 | Missense Mutation | CGT,TGT | R468C | XP_005251740.1 |
| XM_006716947.2 | 1467 | Missense Mutation | CGT,TGT | R434C | XP_006717010.1 |
| XM_011518190.2 | 1467 | Missense Mutation | CGT,TGT | R526C | XP_011516492.1 |
| XM_011518191.2 | 1467 | Missense Mutation | CGT,TGT | R526C | XP_011516493.1 |
| XM_011518192.2 | 1467 | Missense Mutation | CGT,TGT | R526C | XP_011516494.1 |
| XM_011518193.2 | 1467 | Intron | XP_011516495.1 | ||
| XM_017014240.1 | 1467 | Missense Mutation | CGT,TGT | R203C | XP_016869729.1 |