| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001037329.3 | 449 | Missense Mutation | CGC,TGC | R143C | NP_001032406.1 |
| XM_017017217.1 | 449 | Missense Mutation | CGC,TGC | R143C | XP_016872706.1 |
| XM_017017218.1 | 449 | Missense Mutation | CGC,TGC | R103C | XP_016872707.1 |
| XM_017017219.1 | 449 | Missense Mutation | CGC,TGC | R103C | XP_016872708.1 |