| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135608.1 | 529 | Missense Mutation | ACA,ATA | T47I | NP_001129080.1 |
| NM_015071.4 | 529 | Missense Mutation | ACA,ATA | T47I | NP_055886.1 |
| XM_005268398.4 | 529 | Intron | XP_005268455.1 | ||
| XM_005268399.4 | 529 | Intron | XP_005268456.1 | ||
| XM_005268400.4 | 529 | Intron | XP_005268457.1 | ||
| XM_005268402.4 | 529 | Missense Mutation | ACA,ATA | T47I | XP_005268459.1 |
| XM_006714774.3 | 529 | Intron | XP_006714837.1 | ||
| XM_011537610.2 | 529 | Intron | XP_011535912.1 | ||
| XM_011537611.2 | 529 | Intron | XP_011535913.1 | ||
| XM_011537612.2 | 529 | Intron | XP_011535914.1 | ||
| XM_017009247.1 | 529 | Intron | XP_016864736.1 | ||
| XM_017009248.1 | 529 | Intron | XP_016864737.1 | ||
| XM_017009249.1 | 529 | Intron | XP_016864738.1 | ||
| XM_017009250.1 | 529 | Intron | XP_016864739.1 |