| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001291586.1 | 424 | Missense Mutation | ACT,CCT | T47P | NP_001278515.1 |
| NM_001291587.1 | 424 | Intron | NP_001278516.1 | ||
| NM_001291588.1 | 424 | Missense Mutation | ACT,CCT | T47P | NP_001278517.1 |
| NM_145041.3 | 424 | Missense Mutation | ACT,CCT | T47P | NP_659478.1 |
| XM_006721658.2 | 424 | Missense Mutation | ACT,CCT | T47P | XP_006721721.1 |
| XM_006721659.3 | 424 | Intron | XP_006721722.1 | ||
| XM_011524260.1 | 424 | Missense Mutation | ACT,CCT | T47P | XP_011522562.1 |
| XM_017024113.1 | 424 | Missense Mutation | ACT,CCT | T47P | XP_016879602.1 |
| XM_017024114.1 | 424 | Intron | XP_016879603.1 |