| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001018003.2 | 774 | Intron | NP_001018003.1 | ||
| NM_005775.4 | 774 | Missense Mutation | CGC,TGC | R9C | NP_005766.3 |
| XM_005273371.1 | 774 | Intron | XP_005273428.1 | ||
| XM_006716266.1 | 774 | Missense Mutation | CGC,TGC | R63C | XP_006716329.1 |
| XM_006716268.2 | 774 | Missense Mutation | CGC,TGC | R9C | XP_006716331.1 |
| XM_017012944.1 | 774 | Intron | XP_016868433.1 | ||
| XM_017012945.1 | 774 | Intron | XP_016868434.1 | ||
| XM_017012946.1 | 774 | Intron | XP_016868435.1 |