Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006477.4 | 588 | Silent Mutation | TTC,TTT | F26F | NP_006468.1 |
XM_011529821.1 | 588 | Intron | XP_011528123.1 | ||
XM_011529822.1 | 588 | Intron | XP_011528124.1 | ||
XM_011529823.1 | 588 | Intron | XP_011528125.1 |