| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001111101.1 | 997 | Nonsense Mutation | CGA,TGA | R116* | NP_001104571.1 |
| NM_015463.2 | 997 | Intron | NP_056278.1 | ||
| XM_005264249.1 | 997 | Intron | XP_005264306.1 | ||
| XM_006711984.1 | 997 | Intron | XP_006712047.1 |