| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098616.2 | 820 | Missense Mutation | CGC,TGC | R178C | NP_001092086.1 |
| NM_001297717.1 | 820 | Intron | NP_001284646.1 | ||
| NM_001297718.1 | 820 | Missense Mutation | CGC,TGC | R143C | NP_001284647.1 |
| NM_001297720.1 | 820 | Missense Mutation | CGC,TGC | R160C | NP_001284649.1 |
| NM_001297721.1 | 820 | Missense Mutation | CGC,TGC | R144C | NP_001284650.1 |
| NM_001297723.1 | 820 | Missense Mutation | CGC,TGC | R178C | NP_001284652.1 |
| NM_015449.3 | 820 | Missense Mutation | CGC,TGC | R144C | NP_056264.1 |
| NM_138740.3 | 820 | Missense Mutation | CGC,TGC | R126C | NP_620077.1 |