ENST00000539215.6:c.549G>T
|
|
|
ENST00000699982.1:c.1648G>T
|
|
|
ENST00000699983.1:c.1648G>T
|
|
|
ENST00000699984.1:c.1648G>T
|
|
|
ENST00000320574.10:c.1794G>T
MANE Select
|
ENSP00000322570.5:p.Glu598Asp
|
|
ENST00000672742.1:c.*1296G>T
|
ENSP00000500279.1:n.*1296G>T
|
|
ENST00000320574.9:c.1794G>T
|
ENSP00000322570.5:p.Glu598Asp
|
|
ENST00000535270.5:c.1713G>T
|
ENSP00000445753.1:p.Glu571Asp
|
|
ENST00000537064.5:c.*841G>T
|
ENSP00000442578.1:n.*841G>T
|
|
NM_006231.3:c.1794G>T , LRG_789t1:c.1794G>T
|
NP_006222.2:p.Glu598Asp
|
|
XM_011534795.1:c.1794G>T
|
XP_011533097.1:p.Glu598Asp
|
|
XM_011534796.1:c.1665G>T
|
XP_011533098.1:p.Glu555Asp
|
|
XM_011534797.1:c.873G>T
|
XP_011533099.1:p.Glu291Asp
|
|
XM_011534798.1:c.456G>T
|
XP_011533100.1:p.Glu152Asp
|
|
XM_011534799.1:c.1794G>T
|
XP_011533101.1:p.Glu598Asp
|
|
XM_011534800.1:c.1794G>T
|
XP_011533102.1:p.Glu598Asp
|
|
XM_011534801.1:c.1794G>T
|
XP_011533103.1:p.Glu598Asp
|
|
XR_941395.1:n.2003G>T
|
|
|
XM_011534795.3:c.1794G>T
|
XP_011533097.1:p.Glu598Asp
|
|
XM_011534797.3:c.873G>T
|
XP_011533099.1:p.Glu291Asp
|
|
XM_011534799.2:c.1794G>T
|
XP_011533101.1:p.Glu598Asp
|
|
XR_002957338.1:n.1998G>T
|
|
|
XR_002957339.1:n.1998G>T
|
|
|
XR_941395.2:n.1998G>T
|
|
|
NM_006231.4:c.1794G>T
MANE Select
|
NP_006222.2:p.Glu598Asp
|
|