| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301738.1 | 821 | Intron | NP_001288667.1 | ||
| NM_198282.3 | 821 | Missense Mutation | ACC,GCC | T262A | NP_938023.1 |
| XM_005268445.3 | 821 | Intron | XP_005268502.1 | ||
| XM_011537639.2 | 821 | Intron | XP_011535941.1 | ||
| XM_011537640.2 | 821 | Missense Mutation | ACC,GCC | T143A | XP_011535942.1 |