| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001014336.1 | 292 | Missense Mutation | CGG,TGG | R89W | NP_001014358.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098519.1 | 292 | Intron | NP_001091989.1 | ||
| NM_152759.4 | 292 | Intron | NP_689972.3 | ||
| XM_017019124.1 | 292 | Intron | XP_016874613.1 | ||
| XM_017019125.1 | 292 | Intron | XP_016874614.1 |