ENST00000344887.10:c.184G=
MANE Select
|
ENSP00000341838.5:p.Glu62=
|
|
ENST00000665070.1:c.184G=
|
ENSP00000499482.1:p.Glu62=
|
|
ENST00000344887.9:c.184G=
|
ENSP00000341838.5:p.Glu62=
|
|
ENST00000585806.5:n.183G=
|
|
|
ENST00000586669.5:n.192G=
|
|
|
ENST00000586858.1:c.147G=
|
ENSP00000465258.1:p.Trp49=
|
|
ENST00000587176.5:n.368G=
|
|
|
ENST00000587871.1:c.803G=
|
|
|
ENST00000588882.1:c.109G=
|
ENSP00000466729.1:p.Glu37=
|
|
ENST00000590463.1:n.356G=
|
|
|
NM_000363.4:c.184G= , LRG_432t1:c.184G=
|
NP_000354.4:p.Glu62=
|
|
NM_000363.5:c.184G=
MANE Select
|
NP_000354.4:p.Glu62=
|
|