Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135651.2 | 1797 | Missense Mutation | CTT,TTT | L514F | NP_001129123.1 |
NM_001135652.2 | 1797 | Missense Mutation | CTT,TTT | L473F | NP_001129124.1 |
NM_002759.3 | 1797 | Missense Mutation | CTT,TTT | L514F | NP_002750.1 |
XM_011532987.2 | 1797 | Missense Mutation | CTT,TTT | L514F | XP_011531289.1 |
XM_017004503.1 | 1797 | Missense Mutation | CTT,TTT | L471F | XP_016859992.1 |