ENST00000535990.6:c.*104G>T
|
ENSP00000443822.2:n.*104G>T
|
|
ENST00000695924.1:n.575G>T
|
|
|
ENST00000695925.1:n.575G>T
|
|
|
ENST00000695926.1:n.575G>T
|
|
|
ENST00000294053.9:c.504G>T
MANE Plus Clinical
|
ENSP00000294053.3:p.Trp168Cys
|
|
ENST00000535477.6:c.379G>T
|
ENSP00000440423.2:p.Asp127Tyr
|
|
ENST00000538039.6:c.504G>T
MANE Select
|
ENSP00000441518.1:p.Trp168Cys
|
|
ENST00000543042.6:c.504G>T
|
ENSP00000439746.2:p.Trp168Cys
|
|
ENST00000642288.1:c.-10G>T
|
ENSP00000495167.1:n.-10G>T
|
|
ENST00000646117.1:c.504G>T
|
ENSP00000495421.1:p.Trp168Cys
|
|
ENST00000294053.7:c.504G>T
|
ENSP00000294053.3:p.Trp168Cys
|
|
ENST00000340729.9:c.456-22620G>T
|
ENSP00000340385.5:n.456-22620G>T
|
|
ENST00000437826.6:c.369G>T
|
ENSP00000407296.2:p.Trp123Cys
|
|
ENST00000445069.4:n.331G>T
|
|
|
ENST00000535477.5:c.504G>T
|
ENSP00000440423.1:p.Trp168Cys
|
|
ENST00000535990.5:c.519G>T
|
ENSP00000443822.1:p.Trp173Cys
|
|
ENST00000538039.5:c.504G>T
|
ENSP00000441518.1:p.Trp168Cys
|
|
ENST00000539148.3:c.66G>T
|
ENSP00000445327.1:p.Trp22Cys
|
|
ENST00000543042.5:c.-10G>T
|
ENSP00000439746.1:n.-10G>T
|
|
ENST00000544683.5:c.66G>T
|
ENSP00000442651.1:p.Trp22Cys
|
|
NM_001258392.1:c.504G>T
|
NP_001245321.1:p.Trp168Cys
|
|
NM_001258392.2:c.504G>T
|
NP_001245321.1:p.Trp168Cys
|
|
NM_001258393.1:c.456-22620G>T
|
NP_001245322.1:n.456-22620G>T
|
|
NM_001258393.2:c.456-22620G>T
|
NP_001245322.1:n.456-22620G>T
|
|
NM_001258394.1:c.369G>T
|
NP_001245323.1:p.Trp123Cys
|
|
NM_001258394.2:c.369G>T
|
NP_001245323.1:p.Trp123Cys
|
|
NM_030813.4:c.504G>T
|
NP_110440.1:p.Trp168Cys
|
|
NM_030813.5:c.504G>T
|
NP_110440.1:p.Trp168Cys
|
|
XM_005274320.1:c.456-22620G>T
|
XP_005274377.1:n.456-22620G>T
|
|
XM_011545288.1:c.504G>T
|
XP_011543590.1:p.Trp168Cys
|
|
XM_011545289.1:c.504G>T
|
XP_011543591.1:p.Trp168Cys
|
|
XM_011545289.2:c.504G>T
|
XP_011543591.1:p.Trp168Cys
|
|
NM_001258392.3:c.504G>T
MANE Select
|
NP_001245321.1:p.Trp168Cys
|
|
NM_001258393.3:c.456-22620G>T
|
NP_001245322.1:n.456-22620G>T
|
|
NM_030813.6:c.504G>T
MANE Plus Clinical
|
NP_110440.1:p.Trp168Cys
|
|
NM_001258394.3:c.369G>T
|
NP_001245323.1:p.Trp123Cys
|
|