| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001190707.1 | 2815 | Missense Mutation | CGT,TGT | R907C | NP_001177636.1 |
| NM_147129.4 | 2815 | Missense Mutation | CGT,TGT | R907C | NP_667340.2 |
| XM_005265025.1 | 2815 | Missense Mutation | CGT,TGT | R422C | XP_005265082.1 |
| XM_006713091.2 | 2815 | Intron | XP_006713154.1 | ||
| XM_006713093.3 | 2815 | Intron | XP_006713156.1 | ||
| XM_006713094.3 | 2815 | Intron | XP_006713157.1 | ||
| XM_011533572.2 | 2815 | Intron | XP_011531874.1 | ||
| XM_017006120.1 | 2815 | Intron | XP_016861609.1 |