| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001008404.2 | 388 | Missense Mutation | CGT,TGT | R18C | NP_001008404.1 |
| NM_001286399.1 | 388 | Missense Mutation | CGT,TGT | R18C | NP_001273328.1 |
| NM_001286400.1 | 388 | Missense Mutation | CGT,TGT | R18C | NP_001273329.1 |
| XM_005267638.3 | 388 | Missense Mutation | CGT,TGT | R18C | XP_005267695.1 |
| XM_011536764.2 | 388 | Missense Mutation | CGT,TGT | R18C | XP_011535066.1 |