| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000400.3 | 2625 | Intron | NP_000391.1 | ||
| NM_001130867.1 | 2625 | Intron | NP_001124339.1 | ||
| XM_011526611.2 | 2625 | UTR 3 | XP_011524913.1 | ||
| XM_017026467.1 | 2625 | UTR 3 | XP_016881956.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_177417.2 | 2625 | Missense Mutation | CGG,TGG | R492W | NP_803136.2 |