| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001141919.1 | 1447 | Intron | NP_001135391.1 | ||
| NM_001141920.1 | 1447 | Intron | NP_001135392.1 | ||
| NM_175569.2 | 1447 | Intron | NP_780778.1 | ||
| XM_005274587.3 | 1447 | Missense Mutation | CCG,CTG | P99L | XP_005274644.1 |
| XM_011545575.2 | 1447 | Missense Mutation | CCG,CTG | P99L | XP_011543877.1 |
| XM_017029787.1 | 1447 | Missense Mutation | CCG,CTG | P85L | XP_016885276.1 |