| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001099646.1 | 1698 | Missense Mutation | CAG,CGG | Q472R | NP_001093116.1 |
| NM_001256663.1 | 1698 | Missense Mutation | CAG,CGG | Q486R | NP_001243592.1 |
| NM_152908.3 | 1698 | Missense Mutation | CAG,CGG | Q508R | NP_690872.2 |
| XM_017024221.1 | 1698 | Missense Mutation | CAG,CGG | Q522R | XP_016879710.1 |
| XM_017024222.1 | 1698 | Missense Mutation | CAG,CGG | Q473R | XP_016879711.1 |
| XM_017024223.1 | 1698 | Intron | XP_016879712.1 | ||
| XM_017024224.1 | 1698 | Intron | XP_016879713.1 | ||
| XM_017024225.1 | 1698 | Intron | XP_016879714.1 | ||
| XM_017024226.1 | 1698 | Intron | XP_016879715.1 |