| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000263.3 | 777 | Missense Mutation | CGC,TGC | R234C | NP_000254.2 |
| XM_006721920.2 | 777 | UTR 5 | XP_006721983.1 | ||
| XM_011524840.1 | 777 | UTR 5 | XP_011523142.1 | ||
| XM_017024686.1 | 777 | Missense Mutation | CGC,TGC | R31C | XP_016880175.1 |
| XM_017024687.1 | 777 | UTR 5 | XP_016880176.1 |