| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001289107.1 | 1933 | Missense Mutation | CAG,CGG | Q446R | NP_001276036.1 |
| NM_018414.4 | 1933 | Missense Mutation | CAG,CGG | Q578R | NP_060884.1 |
| XM_011524995.2 | 1933 | Intron | XP_011523297.1 | ||
| XM_011524996.2 | 1933 | Intron | XP_011523298.1 | ||
| XM_017024842.1 | 1933 | Intron | XP_016880331.1 | ||
| XM_017024843.1 | 1933 | Intron | XP_016880332.1 | ||
| XM_017024844.1 | 1933 | Intron | XP_016880333.1 |