| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001267571.1 | 2900 | Missense Mutation | CAG,CGG | Q907R | NP_001254500.1 |
| NM_001267572.1 | 2900 | Missense Mutation | CAG,CGG | Q447R | NP_001254501.1 |
| NM_018421.3 | 2900 | Missense Mutation | CAG,CGG | Q896R | NP_060891.3 |
| XM_011518843.1 | 2900 | Missense Mutation | CAG,CGG | Q447R | XP_011517145.1 |
| XM_011518844.2 | 2900 | Intron | XP_011517146.1 | ||
| XM_017014899.1 | 2900 | Missense Mutation | CAG,CGG | Q462R | XP_016870388.1 |