ENST00000682568.1:n.1853A=
|
|
|
ENST00000682617.1:c.1913A=
|
ENSP00000507912.1:p.Glu638=
|
|
ENST00000682826.1:c.*1089A=
|
ENSP00000507274.1:n.*1089A=
|
|
ENST00000682909.1:n.3815A=
|
|
|
ENST00000683277.1:n.3420A=
|
|
|
ENST00000683407.1:n.1783A=
|
|
|
ENST00000683962.1:c.*1469A=
|
ENSP00000506854.1:n.*1469A=
|
|
ENST00000311895.8:c.1775A=
MANE Select
|
ENSP00000310520.7:p.Glu592=
|
|
ENST00000311895.7:c.1775A=
|
ENSP00000310520.7:p.Glu592=
|
|
ENST00000389138.7:n.1052A=
|
|
|
NM_005236.2:c.1775A= , LRG_463t1:c.1775A=
|
NP_005227.1:p.Glu592=
|
|
XM_011522424.1:c.1913A=
|
XP_011520726.1:p.Glu638=
|
|
XM_011522425.1:c.1232A=
|
XP_011520727.1:p.Glu411=
|
|
XM_011522426.1:c.986A=
|
XP_011520728.1:p.Glu329=
|
|
XM_011522427.1:c.425A=
|
XP_011520729.1:p.Glu142=
|
|
XR_932805.1:n.1934A=
|
|
|
XM_011522424.3:c.1913A=
|
XP_011520726.1:p.Glu638=
|
|
XM_017023043.2:c.986A=
|
XP_016878532.1:p.Glu329=
|
|
NM_005236.3:c.1775A=
MANE Select
|
NP_005227.1:p.Glu592=
|
|