Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003268.5 | 2798 | Missense Mutation | CTT,TTT | L769F | NP_003259.2 |
XM_005273241.4 | 2798 | Missense Mutation | CTT,TTT | L769F | XP_005273298.2 |
XM_005273242.4 | 2798 | Missense Mutation | CTT,TTT | L769F | XP_005273299.2 |
XM_005273243.4 | 2798 | Missense Mutation | CTT,TTT | L769F | XP_005273300.2 |
XM_006711504.3 | 2798 | Missense Mutation | CTT,TTT | L769F | XP_006711567.1 |
XM_006711505.3 | 2798 | Missense Mutation | CTT,TTT | L769F | XP_006711568.1 |
XM_006711506.3 | 2798 | Missense Mutation | CTT,TTT | L769F | XP_006711569.1 |
XM_011509937.2 | 2798 | Missense Mutation | CTT,TTT | L769F | XP_011508239.1 |
XM_017002208.1 | 2798 | Missense Mutation | CTT,TTT | L769F | XP_016857697.1 |