| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001319953.1 | 469 | Intron | NP_001306882.1 | ||
| NM_153007.4 | 469 | Missense Mutation | TGG,TTG | W96L | NP_694552.2 |
| XM_005256476.3 | 469 | Intron | XP_005256533.1 | ||
| XM_011523688.1 | 469 | Intron | XP_011521990.1 |