| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001025160.2 | 602 | Missense Mutation | CGT,TGT | R120C | NP_001020331.1 |
| NM_001784.4 | 602 | Intron | NP_001775.2 | ||
| NM_078481.3 | 602 | Missense Mutation | CGT,TGT | R120C | NP_510966.1 |
| XM_011528451.2 | 602 | Missense Mutation | CGT,TGT | R120C | XP_011526753.1 |
| XM_017027547.1 | 602 | Missense Mutation | CGT,TGT | R120C | XP_016883036.1 |