Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002980.2 | 758 | Missense Mutation | CTC,TTC | L387F | NP_002971.2 |
XM_005263730.4 | 758 | Missense Mutation | CTC,TTC | L209F | XP_005263787.1 |
XM_011511621.2 | 758 | Missense Mutation | CTC,TTC | L392F | XP_011509923.1 |
XM_017004670.1 | 758 | Missense Mutation | CTC,TTC | L382F | XP_016860159.1 |
XM_017004671.1 | 758 | Missense Mutation | CTC,TTC | L356F | XP_016860160.1 |
XM_017004672.1 | 758 | Missense Mutation | CTC,TTC | L324F | XP_016860161.1 |
XM_017004673.1 | 758 | Missense Mutation | CTC,TTC | L214F | XP_016860162.1 |