| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002022.2 | 1707 | Intron | NP_002013.1 | ||
| XM_005245045.3 | 1707 | Intron | XP_005245102.1 | ||
| XM_005245046.3 | 1707 | Intron | XP_005245103.1 | ||
| XM_005245048.3 | 1707 | Intron | XP_005245105.1 | ||
| XM_006711243.3 | 1707 | Intron | XP_006711306.1 | ||
| XM_011509347.2 | 1707 | Missense Mutation | ACG,ATG | T425M | XP_011507649.1 |
| XM_011509348.2 | 1707 | Intron | XP_011507650.1 | ||
| XM_011509349.2 | 1707 | Intron | XP_011507651.1 |