| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308440.1 | 890 | Intron | NP_001295369.1 | ||
| NM_020828.1 | 890 | Intron | NP_065879.1 | ||
| XM_011526462.2 | 890 | Intron | XP_011524764.1 | ||
| XM_011526463.2 | 890 | Missense Mutation | CAG,CAT | Q21H | XP_011524765.2 |