| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001079537.1 | 802 | Missense Mutation | CAG,CGG | Q156R | NP_001073005.1 |
| NM_177452.3 | 802 | Missense Mutation | CAG,CGG | Q128R | NP_803235.1 |
| XM_011536409.2 | 802 | Missense Mutation | CAG,CGG | Q118R | XP_011534711.1 |
| XM_017020964.1 | 802 | Intron | XP_016876453.1 |