| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013323.2 | 448 | Missense Mutation | CGT,TGT | R61C | NP_037455.2 |
| NM_152244.1 | 448 | Missense Mutation | CGT,TGT | R61C | NP_689450.1 |
| XM_005257260.3 | 448 | Missense Mutation | CGT,TGT | R61C | XP_005257317.1 |
| XM_005257261.3 | 448 | Missense Mutation | CGT,TGT | R53C | XP_005257318.1 |
| XM_005257262.3 | 448 | Missense Mutation | CGT,TGT | R53C | XP_005257319.1 |
| XM_011524697.2 | 448 | Missense Mutation | CGT,TGT | R61C | XP_011522999.1 |