| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_145276.2 | 527 | Missense Mutation | CGT,TGT | R97C | NP_660319.1 |
| XM_005259750.4 | 527 | Intron | XP_005259807.1 | ||
| XM_005259751.3 | 527 | Intron | XP_005259808.1 | ||
| XM_006722650.3 | 527 | Intron | XP_006722713.1 | ||
| XM_006722651.3 | 527 | Intron | XP_006722714.1 | ||
| XM_011527698.1 | 527 | Intron | XP_011526000.1 | ||
| XM_011527699.2 | 527 | Missense Mutation | CGT,TGT | R60C | XP_011526001.1 |
| XM_011527700.2 | 527 | Intron | XP_011526002.1 | ||
| XM_017026332.1 | 527 | Intron | XP_016881821.1 |