| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320350.1 | 655 | Silent Mutation | TTC,TTT | F50F | NP_001307279.1 |
| NM_001320351.1 | 655 | Silent Mutation | TTC,TTT | F50F | NP_001307280.1 |
| NM_001320352.1 | 655 | Intron | NP_001307281.1 | ||
| NM_003307.3 | 655 | Silent Mutation | TTC,TTT | F50F | NP_003298.1 |
| XM_005261171.3 | 655 | Missense Mutation | TTC,TTT | F50F | XP_005261228.1 |
| XM_011529736.2 | 655 | Missense Mutation | TTC,TTT | F50F | XP_011528038.1 |
| XM_017028456.1 | 655 | Missense Mutation | TTC,TTT | F50F | XP_016883945.1 |
| XM_017028457.1 | 655 | Missense Mutation | TTC,TTT | F50F | XP_016883946.1 |