| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000016.5 | 452 | Missense Mutation | GGG,GTG | G4V | NP_000007.1 |
| NM_001127328.2 | 452 | Missense Mutation | GGG,GTG | G4V | NP_001120800.1 |
| NM_001286042.1 | 452 | UTR 5 | NP_001272971.1 | ||
| NM_001286043.1 | 452 | Missense Mutation | GGG,GTG | G4V | NP_001272972.1 |
| NM_001286044.1 | 452 | UTR 5 | NP_001272973.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130058.1 | 452 | Intron | NP_001123530.1 | ||
| NM_001320283.1 | 452 | Intron | NP_001307212.1 | ||
| NM_001320285.1 | 452 | Intron | NP_001307214.1 | ||
| NM_001320287.1 | 452 | Intron | NP_001307216.1 | ||
| NM_152697.4 | 452 | Intron | NP_689910.2 | ||
| XM_006710445.3 | 452 | Intron | XP_006710508.1 | ||
| XM_011540986.2 | 452 | Intron | XP_011539288.1 | ||
| XM_011540987.2 | 452 | Intron | XP_011539289.1 | ||
| XM_017000607.1 | 452 | Intron | XP_016856096.1 | ||
| XM_017000608.1 | 452 | Intron | XP_016856097.1 | ||
| XM_017000609.1 | 452 | Intron | XP_016856098.1 | ||
| XM_017000610.1 | 452 | Intron | XP_016856099.1 | ||
| XM_017000611.1 | 452 | Intron | XP_016856100.1 |