|
ENST00000371068.11:c.942A>C
MANE Select
|
ENSP00000360107.4:p.Glu314Asp
|
|
|
ENST00000480623.6:c.942A>C
|
ENSP00000434498.2:p.Glu314Asp
|
|
|
ENST00000635760.1:c.618A>C
|
ENSP00000489765.1:p.Glu206Asp
|
|
|
ENST00000635812.1:c.*243A>C
|
ENSP00000490859.1:n.*243A>C
|
|
|
ENST00000635866.1:c.*811A>C
|
ENSP00000489866.1:n.*811A>C
|
|
|
ENST00000635911.1:n.2460A>C
|
|
|
|
ENST00000635984.1:c.618A>C
|
ENSP00000489921.1:p.Glu206Asp
|
|
|
ENST00000635996.1:c.942A>C
|
ENSP00000490256.1:p.Glu314Asp
|
|
|
ENST00000636107.1:c.942A>C
|
ENSP00000489680.1:p.Glu314Asp
|
|
|
ENST00000636311.1:n.836A>C
|
|
|
|
ENST00000636343.1:c.608A>C
|
|
|
|
ENST00000636379.1:c.654A>C
|
ENSP00000490622.1:p.Glu218Asp
|
|
|
ENST00000636398.1:c.642A>C
|
ENSP00000489654.1:n.642A>C
|
|
|
ENST00000636489.1:c.885A>C
|
ENSP00000489998.1:p.Glu295Asp
|
|
|
ENST00000636616.1:n.558A>C
|
|
|
|
ENST00000636702.1:c.912A>C
|
ENSP00000489623.1:p.Glu304Asp
|
|
|
ENST00000636954.1:c.885A>C
|
ENSP00000489966.1:p.Glu295Asp
|
|
|
ENST00000637089.1:c.942A>C
|
ENSP00000489854.1:p.Glu314Asp
|
|
|
ENST00000637263.1:c.942A>C
|
ENSP00000489700.1:p.Glu314Asp
|
|
|
ENST00000637340.1:n.2867A>C
|
|
|
|
ENST00000637353.1:c.942A>C
|
ENSP00000490441.1:p.Glu314Asp
|
|
|
ENST00000637602.1:c.*643A>C
|
ENSP00000490074.1:n.*643A>C
|
|
|
ENST00000637849.1:n.1006A>C
|
|
|
|
ENST00000637874.1:c.83-4413A>C
|
ENSP00000490348.1:n.83-4413A>C
|
|
|
ENST00000637892.1:n.1146A>C
|
|
|
|
ENST00000371068.9:c.942A>C
|
ENSP00000360107.4:p.Glu314Asp
|
|
|
ENST00000480623.5:c.*1362A>C
|
ENSP00000434498.1:n.*1362A>C
|
|
|
ENST00000538167.2:c.885A>C
|
ENSP00000444521.1:p.Glu295Asp
|
|
|
NM_001172420.1:c.885A>C
|
NP_001165891.1:p.Glu295Asp
|
|
|
NM_018100.3:c.942A>C
|
NP_060570.2:p.Glu314Asp
|
|
|
NR_033327.1:n.2414A>C
|
|
|
|
NM_018100.4:c.942A>C
MANE Select
|
NP_060570.2:p.Glu314Asp
|
|
|
NM_001172420.2:c.885A>C
|
NP_001165891.1:p.Glu295Asp
|
|
|
NR_033327.2:n.2268A>C
|
|
|
