Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_177538.2 | 805 | Missense Mutation | TTG,TTT | L61F | NP_803882.1 |
XM_005246698.3 | 805 | Intron | XP_005246755.1 | ||
XM_005246699.3 | 805 | Intron | XP_005246756.1 | ||
XM_005246701.3 | 805 | Intron | XP_005246758.1 | ||
XM_006712644.3 | 805 | Missense Mutation | TTG,TTT | L43F | XP_006712707.1 |
XM_006712645.3 | 805 | Missense Mutation | TTG,TTT | L61F | XP_006712708.1 |
XM_017004555.1 | 805 | Intron | XP_016860044.1 |