| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000921.4 | 736 | Silent Mutation | TTC,TTT | F232F | NP_000912.3 |
| NM_001244683.1 | 736 | Intron | NP_001231612.1 | ||
| XM_017019420.1 | 736 | Missense Mutation | TTC,TTT | F232F | XP_016874909.1 |
| XM_017019421.1 | 736 | Intron | XP_016874910.1 |