| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001277155.2 | 1789 | Intron | NP_001264084.1 | ||
| NM_152490.4 | 1789 | Silent Mutation | TGC,TGT | C491C | NP_689703.1 |
| XM_006711749.3 | 1789 | Intron | XP_006711812.1 | ||
| XM_017000394.1 | 1789 | Silent Mutation | TGC,TGT | C532C | XP_016855883.1 |
| XM_017000395.1 | 1789 | UTR 3 | XP_016855884.1 |