Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001382.3 | 1749 | Missense Mutation | CTT,TTT | L371F | NP_001373.2 |
XM_005271422.2 | 1749 | Missense Mutation | CTT,TTT | L371F | XP_005271479.1 |
XM_011542648.1 | 1749 | Missense Mutation | CTT,TTT | L264F | XP_011540950.1 |
XM_017017293.1 | 1749 | Missense Mutation | CTT,TTT | L264F | XP_016872782.1 |
XM_017017294.1 | 1749 | UTR 3 | XP_016872783.1 | ||
XM_017017295.1 | 1749 | Missense Mutation | CTT,TTT | L199F | XP_016872784.1 |