ENST00000588860.6:c.1614A>T
|
ENSP00000465878.2:p.Glu538Asp
|
|
ENST00000589076.6:c.1614A>T
|
ENSP00000466934.2:p.Glu538Asp
|
|
ENST00000589941.2:c.1614A>T
|
ENSP00000465874.2:p.Glu538Asp
|
|
ENST00000590061.2:c.1614A>T
|
ENSP00000464772.2:p.Glu538Asp
|
|
ENST00000593223.2:c.*1611A>T
|
ENSP00000466118.2:n.*1611A>T
|
|
ENST00000611848.2:c.*266A>T
|
ENSP00000478613.2:n.*266A>T
|
|
ENST00000684953.1:n.3629A>T
|
|
|
ENST00000685090.1:n.3544A>T
|
|
|
ENST00000685232.1:n.1835A>T
|
|
|
ENST00000688574.1:n.1722A>T
|
|
|
ENST00000691124.1:n.4575A>T
|
|
|
ENST00000342988.8:c.1614A>T
MANE Select
|
ENSP00000341551.3:p.Glu538Asp
|
|
ENST00000342988.7:c.1614A>T
|
ENSP00000341551.3:p.Glu538Asp
|
|
ENST00000398417.6:c.1614A>T
|
ENSP00000381452.1:p.Glu538Asp
|
|
ENST00000586253.1:n.336A>T
|
|
|
ENST00000588745.5:c.1326A>T
|
ENSP00000464901.1:p.Glu442Asp
|
|
ENST00000591126.5:n.3615A>T
|
|
|
ENST00000592186.5:c.1261A>T
|
ENSP00000468611.1:n.1261A>T
|
|
ENST00000611848.1:c.927A>T
|
|
|
NM_005359.5:c.1614A>T , LRG_318t1:c.1614A>T
|
NP_005350.1:p.Glu538Asp
|
|
NM_005359.6:c.1614A>T
MANE Select
|
NP_005350.1:p.Glu538Asp
|
|