| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271609.1 | 896 | Intron | NP_001258538.1 | ||
| NM_001271610.1 | 896 | Missense Mutation | GGT,GTT | G232V | NP_001258539.1 |
| NM_001271611.1 | 896 | Intron | NP_001258540.1 | ||
| NM_003765.2 | 896 | Intron | NP_003756.1 | ||
| XM_011528397.2 | 896 | Intron | XP_011526699.1 |