ENST00000487848.6:c.1296C>A
MANE Plus Clinical
|
ENSP00000417074.1:p.Ala432=
|
|
ENST00000696466.1:c.1578C>A
|
ENSP00000512647.1:p.Ala526=
|
|
ENST00000696672.1:c.271C>A
|
ENSP00000512796.1:p.Pro91Thr
|
|
ENST00000341105.7:c.1296C>A
MANE Select
|
ENSP00000345681.2:p.Ala432=
|
|
ENST00000341105.6:c.1296C>A
|
ENSP00000345681.2:p.Ala432=
|
|
ENST00000430265.6:c.1254C>A
|
ENSP00000400259.2:p.Ala418=
|
|
ENST00000487848.5:c.1296C>A
|
ENSP00000417074.1:p.Ala432=
|
|
ENST00000489987.1:n.413C>A
|
|
|
NM_001145661.1:c.1296C>A , LRG_295t1:c.1296C>A
|
NP_001139133.1:p.Ala432=
|
|
NM_001145662.1:c.1254C>A
|
NP_001139134.1:p.Ala418=
|
|
NM_032638.4:c.1296C>A , LRG_295t2:c.1296C>A
|
NP_116027.2:p.Ala432=
|
|
NM_001145661.2:c.1296C>A
MANE Plus Clinical
|
NP_001139133.1:p.Ala432=
|
|
NM_032638.5:c.1296C>A
MANE Select
|
NP_116027.2:p.Ala432=
|
|