| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001099676.2 | 1179 | Nonsense Mutation | TGA,TGC | *393C | NP_001093146.1 |
| NM_001170633.1 | 1179 | Nonsense Mutation | TGA,TGC | *553C | NP_001164104.1 |
| XM_017018770.1 | 1179 | Intron | XP_016874259.1 |