| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001322340.1 | 2018 | Missense Mutation | CGT,TGT | R715C | NP_001309269.1 |
| NM_001322341.1 | 2018 | Missense Mutation | CGT,TGT | R692C | NP_001309270.1 |
| NM_001322342.1 | 2018 | Missense Mutation | CGT,TGT | R611C | NP_001309271.1 |
| NM_001322343.1 | 2018 | Missense Mutation | CGT,TGT | R659C | NP_001309272.1 |
| NM_001322344.1 | 2018 | Intron | NP_001309273.1 | ||
| NM_022779.8 | 2018 | Missense Mutation | CGT,TGT | R788C | NP_073616.6 |
| NM_138620.1 | 2018 | Intron | NP_619526.1 | ||
| XM_005272207.4 | 2018 | Missense Mutation | CGT,TGT | R692C | XP_005272264.1 |
| XM_006717236.3 | 2018 | UTR 3 | XP_006717299.1 | ||
| XM_011518921.2 | 2018 | Intron | XP_011517223.1 | ||
| XM_011518922.2 | 2018 | Intron | XP_011517224.1 |