ENST00000326003.7:c.492G=
MANE Select
|
ENSP00000314151.1:p.Glu164=
|
|
ENST00000326003.6:c.492G=
|
ENSP00000314151.1:p.Glu164=
|
|
ENST00000360617.7:c.492G=
|
ENSP00000353829.2:p.Glu164=
|
|
ENST00000422986.6:c.*148G=
|
ENSP00000393628.2:n.*148G=
|
|
ENST00000593997.5:c.492G=
|
ENSP00000472907.1:p.Glu164=
|
|
ENST00000595392.5:c.368G=
|
ENSP00000468912.1:p.Ser123=
|
|
ENST00000595952.5:c.363G=
|
ENSP00000471155.1:p.Glu121=
|
|
ENST00000596185.5:c.*600G=
|
ENSP00000471648.1:n.*600G=
|
|
ENST00000596333.1:n.527G=
|
|
|
ENST00000597286.5:c.381G=
|
ENSP00000470523.1:p.Glu127=
|
|
ENST00000597483.5:c.363G=
|
ENSP00000472411.1:p.Glu121=
|
|
ENST00000598145.1:c.476G=
|
|
|
ENST00000601349.5:n.1771G=
|
|
|
ENST00000601503.5:c.435G=
|
ENSP00000472213.1:p.Glu145=
|
|
ENST00000601812.1:n.924G=
|
|
|
ENST00000617027.4:c.369G=
|
ENSP00000483513.1:p.Glu123=
|
|
NM_001030047.1:c.492G=
|
NP_001025218.1:p.Glu164=
|
|
NM_001030048.1:c.363G=
|
NP_001025219.1:p.Glu121=
|
|
NM_001648.2:c.492G=
MANE Select
|
NP_001639.1:p.Glu164=
|
|
XM_011526923.1:c.492G=
|
XP_011525225.1:p.Glu164=
|
|
XM_011526924.1:c.492G=
|
XP_011525226.1:p.Glu164=
|
|
XR_935817.1:n.527G=
|
|
|