| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000873.3 | 706 | Intron | NP_000864.2 | ||
| NM_001099786.1 | 706 | Intron | NP_001093256.1 | ||
| NM_001099787.1 | 706 | Intron | NP_001093257.1 | ||
| NM_001099788.1 | 706 | Intron | NP_001093258.1 | ||
| NM_001099789.1 | 706 | Intron | NP_001093259.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001164257.1 | 706 | UTR 3 | NP_001157729.1 | ||
| NM_001191029.1 | 706 | Missense Mutation | CAG,CGG | Q231R | NP_001177958.1 |
| NM_001191030.1 | 706 | UTR 3 | NP_001177959.1 | ||
| NM_001191031.1 | 706 | UTR 3 | NP_001177960.1 | ||
| XM_005257805.4 | 706 | UTR 3 | XP_005257862.1 | ||
| XM_011525468.2 | 706 | Missense Mutation | CAG,CGG | Q209R | XP_011523770.1 |
| XM_011525469.1 | 706 | UTR 3 | XP_011523771.1 | ||
| XM_017025315.1 | 706 | Missense Mutation | CAG,CGG | Q144R | XP_016880804.1 |