| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024940.2 | 2285 | Missense Mutation | TTC,TTG | F456L | NP_001020111.1 |
| NM_001134855.1 | 2285 | Intron | NP_001128327.1 | ||
| NM_016102.3 | 2285 | Missense Mutation | TTC,TTG | F456L | NP_057186.1 |
| XM_006711779.2 | 2285 | Missense Mutation | TTC,TTG | F456L | XP_006711842.1 |
| XM_011544209.2 | 2285 | Missense Mutation | TTC,TTG | F456L | XP_011542511.1 |
| XM_011544210.2 | 2285 | Missense Mutation | TTC,TTG | F456L | XP_011542512.1 |
| XM_011544211.2 | 2285 | Missense Mutation | TTC,TTG | F429L | XP_011542513.1 |
| XM_017001418.1 | 2285 | UTR 3 | XP_016856907.1 | ||
| XM_017001419.1 | 2285 | UTR 3 | XP_016856908.1 |