| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145349.1 | 1627 | Silent Mutation | TGC,TGT | C527C | NP_001138821.1 |
| NM_005897.2 | 1627 | Silent Mutation | TGC,TGT | C527C | NP_005888.1 |
| XM_005270839.4 | 1627 | UTR 3 | XP_005270896.1 | ||
| XM_006710623.3 | 1627 | UTR 3 | XP_006710686.1 | ||
| XM_011541394.2 | 1627 | Intron | XP_011539696.1 | ||
| XM_017001210.1 | 1627 | Intron | XP_016856699.1 |