Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004870.3 | 132 | Missense Mutation | CTC,GTC | L41V | NP_004861.2 |
XM_006721597.2 | 132 | Missense Mutation | CTC,GTC | L41V | XP_006721660.1 |
XM_006721598.2 | 132 | Missense Mutation | CTC,GTC | L41V | XP_006721661.1 |
XM_006721599.2 | 132 | Missense Mutation | CTC,GTC | L41V | XP_006721662.1 |
XM_011524081.2 | 132 | UTR 5 | XP_011522383.1 |