| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015103.2 | 5321 | Missense Mutation | CAG,CGG | Q1899R | NP_055918.2 |
| XM_011512588.1 | 5321 | UTR 3 | XP_011510890.1 | ||
| XM_011512589.1 | 5321 | Missense Mutation | CAG,CGG | Q1769R | XP_011510891.1 |
| XM_011512590.2 | 5321 | Intron | XP_011510892.1 | ||
| XM_011512592.1 | 5321 | Missense Mutation | CAG,CGG | Q955R | XP_011510894.1 |