| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001305121.1 | 712 | UTR 5 | NP_001292050.1 | ||
| NM_001305122.1 | 712 | Missense Mutation | CGG,TGG | R5W | NP_001292051.1 |
| NM_153208.2 | 712 | Missense Mutation | CGG,TGG | R5W | NP_694940.1 |
| XM_011545736.2 | 712 | Intron | XP_011544038.1 | ||
| XM_017022933.1 | 712 | Missense Mutation | CGG,TGG | R5W | XP_016878422.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001012991.2 | 712 | Intron | NP_001013009.2 | ||
| XM_005255317.4 | 712 | Intron | XP_005255374.1 | ||
| XM_006721046.3 | 712 | Intron | XP_006721109.1 | ||
| XM_011545855.1 | 712 | Intron | XP_011544157.1 | ||
| XM_017023231.1 | 712 | Intron | XP_016878720.1 | ||
| XM_017023232.1 | 712 | Intron | XP_016878721.1 |