| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193308.1 | 516 | Missense Mutation | CGC,TGC | R107C | NP_001180237.1 |
| NM_032872.2 | 516 | Missense Mutation | CGC,TGC | R107C | NP_116261.1 |
| XM_005246022.3 | 516 | Missense Mutation | CGC,TGC | R139C | XP_005246079.1 |
| XM_006710990.1 | 516 | Missense Mutation | CGC,TGC | R139C | XP_006711053.1 |
| XM_006710991.1 | 516 | UTR 5 | XP_006711054.1 |