Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032832.5 | 1725 | Silent Mutation | CTC,CTT | L467L | NP_116221.3 |
XM_011536194.2 | 1725 | Silent Mutation | CTC,CTT | L435L | XP_011534496.1 |
XM_017011380.1 | 1725 | Intron | XP_016866869.1 |