| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000677.3 | 1438 | Missense Mutation | CAG,CGG | Q224R | NP_000668.1 |
| NM_001302678.1 | 1438 | UTR 3 | NP_001289607.1 | ||
| NM_001302679.1 | 1438 | Missense Mutation | CAG,CGG | Q79R | NP_001289608.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001081976.2 | 1438 | Intron | NP_001075445.1 | ||
| NM_001302680.1 | 1438 | Intron | NP_001289609.1 | ||
| NM_020683.6 | 1438 | Intron | NP_065734.5 |