| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001083909.2 | 178 | Intron | NP_001077378.1 | ||
| NM_001291085.1 | 178 | Intron | NP_001278014.1 | ||
| XM_005252695.1 | 178 | Missense Mutation | CGG,GGG | R60G | XP_005252752.1 |
| XM_011540273.1 | 178 | Intron | XP_011538575.1 | ||
| XM_017016779.1 | 178 | Intron | XP_016872268.1 |