Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_052897.3 | 479 | Missense Mutation | CTT,TTT | L68F | NP_443129.3 |
XM_005268617.1 | 479 | Missense Mutation | CTT,TTT | L68F | XP_005268674.1 |
XM_005268618.1 | 479 | Missense Mutation | CTT,TTT | L68F | XP_005268675.1 |
XM_005268620.2 | 479 | Missense Mutation | CTT,TTT | L68F | XP_005268677.1 |
XM_006719217.1 | 479 | Missense Mutation | CTT,TTT | L68F | XP_006719280.1 |
XM_006719218.1 | 479 | Missense Mutation | CTT,TTT | L68F | XP_006719281.1 |
XM_011537851.2 | 479 | Missense Mutation | CTT,TTT | L68F | XP_011536153.1 |