| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002980.2 | 766 | Nonsense Mutation | TGA,TGC | *389C | NP_002971.2 |
| XM_005263730.4 | 766 | Nonsense Mutation | TGA,TGC | *211C | XP_005263787.1 |
| XM_011511621.2 | 766 | Nonsense Mutation | TGA,TGC | *394C | XP_011509923.1 |
| XM_017004670.1 | 766 | Nonsense Mutation | TGA,TGC | *384C | XP_016860159.1 |
| XM_017004671.1 | 766 | Nonsense Mutation | TGA,TGC | *358C | XP_016860160.1 |
| XM_017004672.1 | 766 | Nonsense Mutation | TGA,TGC | *326C | XP_016860161.1 |
| XM_017004673.1 | 766 | Nonsense Mutation | TGA,TGC | *216C | XP_016860162.1 |