| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001267571.1 | 2667 | Silent Mutation | TTC,TTT | F829F | NP_001254500.1 |
| NM_001267572.1 | 2667 | Silent Mutation | TTC,TTT | F369F | NP_001254501.1 |
| NM_018421.3 | 2667 | Intron | NP_060891.3 | ||
| XM_011518843.1 | 2667 | Silent Mutation | TTC,TTT | F369F | XP_011517145.1 |
| XM_011518844.2 | 2667 | Intron | XP_011517146.1 | ||
| XM_017014899.1 | 2667 | Silent Mutation | TTC,TTT | F384F | XP_016870388.1 |