| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002020.4 | 4495 | Intron | NP_002011.2 | ||
| NM_182925.4 | 4495 | Missense Mutation | CAG,CGG | Q1320R | NP_891555.2 |
| XM_011534478.2 | 4495 | Missense Mutation | CAG,CGG | Q1397R | XP_011532780.1 |
| XM_011534484.2 | 4495 | Missense Mutation | CAG,CGG | Q1167R | XP_011532786.1 |
| XM_017009263.1 | 4495 | UTR 3 | XP_016864752.1 | ||
| XM_017009264.1 | 4495 | Intron | XP_016864753.1 | ||
| XM_017009265.1 | 4495 | Intron | XP_016864754.1 | ||
| XM_017009266.1 | 4495 | Intron | XP_016864755.1 | ||
| XM_017009267.1 | 4495 | Intron | XP_016864756.1 | ||
| XM_017009268.1 | 4495 | Missense Mutation | CAG,CGG | Q1294R | XP_016864757.1 |