| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001166663.1 | 1294 | Nonsense Mutation | CGA,TGA | R357* | NP_001160135.1 |
| NM_001166664.1 | 1294 | Nonsense Mutation | CGA,TGA | R260* | NP_001160136.1 |
| NM_016382.3 | 1294 | Nonsense Mutation | CGA,TGA | R352* | NP_057466.1 |
| XM_011509621.2 | 1294 | Intron | XP_011507923.1 | ||
| XM_011509622.2 | 1294 | Intron | XP_011507924.1 | ||
| XM_011509623.2 | 1294 | Nonsense Mutation | CGA,TGA | R154* | XP_011507925.1 |