ENST00000344887.10:c.178G=
MANE Select
|
ENSP00000341838.5:p.Glu60=
|
|
ENST00000665070.1:c.178G=
|
ENSP00000499482.1:p.Glu60=
|
|
ENST00000344887.9:c.178G=
|
ENSP00000341838.5:p.Glu60=
|
|
ENST00000585806.5:n.177G=
|
|
|
ENST00000586669.5:n.186G=
|
|
|
ENST00000586858.1:c.141G=
|
ENSP00000465258.1:p.Lys47=
|
|
ENST00000587176.5:n.362G=
|
|
|
ENST00000587871.1:c.797G=
|
|
|
ENST00000588882.1:c.103G=
|
ENSP00000466729.1:p.Glu35=
|
|
ENST00000590463.1:n.350G=
|
|
|
NM_000363.4:c.178G= , LRG_432t1:c.178G=
|
NP_000354.4:p.Glu60=
|
|
NM_000363.5:c.178G=
MANE Select
|
NP_000354.4:p.Glu60=
|
|