ENST00000539215.6:c.181G>T
|
|
|
ENST00000545015.2:n.1500G>T
|
|
|
ENST00000699982.1:c.1327G>T
|
|
|
ENST00000699983.1:c.1327G>T
|
|
|
ENST00000699984.1:c.1327G>T
|
|
|
ENST00000320574.10:c.1473G>T
MANE Select
|
ENSP00000322570.5:p.Glu491Asp
|
|
ENST00000672742.1:c.*975G>T
|
ENSP00000500279.1:n.*975G>T
|
|
ENST00000320574.9:c.1473G>T
|
ENSP00000322570.5:p.Glu491Asp
|
|
ENST00000535270.5:c.1392G>T
|
ENSP00000445753.1:p.Glu464Asp
|
|
ENST00000535934.2:n.1348G>T
|
|
|
ENST00000537064.5:c.*520G>T
|
ENSP00000442578.1:n.*520G>T
|
|
ENST00000539215.5:n.181G>T
|
|
|
ENST00000545015.1:n.70G>T
|
|
|
NM_006231.3:c.1473G>T , LRG_789t1:c.1473G>T
|
NP_006222.2:p.Glu491Asp
|
|
XM_011534795.1:c.1473G>T
|
XP_011533097.1:p.Glu491Asp
|
|
XM_011534796.1:c.1344G>T
|
XP_011533098.1:p.Glu448Asp
|
|
XM_011534797.1:c.552G>T
|
XP_011533099.1:p.Glu184Asp
|
|
XM_011534798.1:c.135G>T
|
XP_011533100.1:p.Glu45Asp
|
|
XM_011534799.1:c.1473G>T
|
XP_011533101.1:p.Glu491Asp
|
|
XM_011534800.1:c.1473G>T
|
XP_011533102.1:p.Glu491Asp
|
|
XM_011534801.1:c.1473G>T
|
XP_011533103.1:p.Glu491Asp
|
|
XR_941395.1:n.1682G>T
|
|
|
XM_011534795.3:c.1473G>T
|
XP_011533097.1:p.Glu491Asp
|
|
XM_011534797.3:c.552G>T
|
XP_011533099.1:p.Glu184Asp
|
|
XM_011534799.2:c.1473G>T
|
XP_011533101.1:p.Glu491Asp
|
|
XR_002957338.1:n.1677G>T
|
|
|
XR_002957339.1:n.1677G>T
|
|
|
XR_941395.2:n.1677G>T
|
|
|
NM_006231.4:c.1473G>T
MANE Select
|
NP_006222.2:p.Glu491Asp
|
|