| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_052935.4 | 790 | Missense Mutation | ACC,GCC | T238A | NP_443167.4 |
| XM_006721669.3 | 790 | Missense Mutation | ACC,GCC | T195A | XP_006721732.1 |
| XM_006721670.3 | 790 | Missense Mutation | ACC,GCC | T195A | XP_006721733.1 |
| XM_011524276.2 | 790 | Intron | XP_011522578.1 | ||
| XM_011524277.2 | 790 | Intron | XP_011522579.1 | ||
| XM_017024127.1 | 790 | Nonsense Mutation | TGA,TGG | *183W | XP_016879616.1 |