| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018117.11 | 41 | Missense Mutation | TTC,TTG | F8L | NP_060587.8 |
| XM_005269962.2 | 41 | Intron | XP_005270019.1 | ||
| XM_005269963.2 | 41 | UTR 5 | XP_005270020.1 | ||
| XM_005269964.2 | 41 | Intron | XP_005270021.1 | ||
| XM_017016397.1 | 41 | Missense Mutation | TTC,TTG | F8L | XP_016871886.1 |
| XM_017016398.1 | 41 | UTR 5 | XP_016871887.1 | ||
| XM_017016399.1 | 41 | UTR 5 | XP_016871888.1 | ||
| XM_017016400.1 | 41 | Missense Mutation | TTC,TTG | F8L | XP_016871889.1 |