ENST00000344887.10:c.180G=
MANE Select
|
ENSP00000341838.5:p.Glu60=
|
|
ENST00000665070.1:c.180G=
|
ENSP00000499482.1:p.Glu60=
|
|
ENST00000344887.9:c.180G=
|
ENSP00000341838.5:p.Glu60=
|
|
ENST00000585806.5:n.179G=
|
|
|
ENST00000586669.5:n.188G=
|
|
|
ENST00000586858.1:c.143G=
|
ENSP00000465258.1:p.Ser48=
|
|
ENST00000587176.5:n.364G=
|
|
|
ENST00000587871.1:c.799G=
|
|
|
ENST00000588882.1:c.105G=
|
ENSP00000466729.1:p.Glu35=
|
|
ENST00000590463.1:n.352G=
|
|
|
NM_000363.4:c.180G= , LRG_432t1:c.180G=
|
NP_000354.4:p.Glu60=
|
|
NM_000363.5:c.180G=
MANE Select
|
NP_000354.4:p.Glu60=
|
|