ENST00000324856.13:c.5358G>T
MANE Select
|
ENSP00000320485.7:p.Glu1786Asp
|
|
ENST00000374152.7:c.4209G>T
|
ENSP00000363267.2:p.Glu1403Asp
|
|
ENST00000430799.7:c.4206G>T
|
ENSP00000390317.3:p.Glu1402Asp
|
|
ENST00000466382.2:c.775G>T
|
|
|
ENST00000636219.1:c.4212G>T
|
ENSP00000489842.1:p.Glu1404Asp
|
|
ENST00000637788.1:n.1158G>T
|
|
|
ENST00000324856.11:c.5358G>T
|
ENSP00000320485.7:p.Glu1786Asp
|
|
ENST00000374152.6:c.4209G>T
|
ENSP00000363267.2:p.Glu1403Asp
|
|
ENST00000430799.6:c.2047G>T
|
|
|
ENST00000457599.6:c.4707G>T
|
ENSP00000387636.2:p.Glu1569Asp
|
|
ENST00000466382.1:c.775G>T
|
|
|
ENST00000532781.1:c.856G>T
|
|
|
NM_006015.4:c.5358G>T , LRG_875t1:c.5358G>T
|
NP_006006.3:p.Glu1786Asp
|
|
NM_139135.2:c.4707G>T
|
NP_624361.1:p.Glu1569Asp
|
|
NM_006015.5:c.5358G>T
|
NP_006006.3:p.Glu1786Asp
|
|
NM_139135.3:c.4707G>T
|
NP_624361.1:p.Glu1569Asp
|
|
NM_006015.6:c.5358G>T
MANE Select
|
NP_006006.3:p.Glu1786Asp
|
|
NM_139135.4:c.4707G>T
|
NP_624361.1:p.Glu1569Asp
|
|