ENST00000588860.6:c.1158T>G
|
ENSP00000465878.2:p.Gly386=
|
|
ENST00000589076.6:c.1158T>G
|
ENSP00000466934.2:p.Gly386=
|
|
ENST00000589941.2:c.1158T>G
|
ENSP00000465874.2:p.Gly386=
|
|
ENST00000590061.2:c.1158T>G
|
ENSP00000464772.2:p.Gly386=
|
|
ENST00000593223.2:c.1158T>G
|
ENSP00000466118.2:p.Gly386=
|
|
ENST00000611848.2:c.1158T>G
|
ENSP00000478613.2:p.Gly386=
|
|
ENST00000684953.1:n.2530T>G
|
|
|
ENST00000685090.1:n.1609T>G
|
|
|
ENST00000685232.1:n.1266T>G
|
|
|
ENST00000688574.1:n.1266T>G
|
|
|
ENST00000691124.1:n.2640T>G
|
|
|
ENST00000342988.8:c.1158T>G
MANE Select
|
ENSP00000341551.3:p.Gly386=
|
|
ENST00000342988.7:c.1158T>G
|
ENSP00000341551.3:p.Gly386=
|
|
ENST00000398417.6:c.1158T>G
|
ENSP00000381452.1:p.Gly386=
|
|
ENST00000588745.5:c.870T>G
|
ENSP00000464901.1:p.Gly290=
|
|
ENST00000590499.1:n.216T>G
|
|
|
ENST00000591126.5:n.3159T>G
|
|
|
ENST00000592186.5:c.955+7121T>G
|
ENSP00000468611.1:n.955+7121T>G
|
|
ENST00000611848.1:c.358T>G
|
|
|
NM_005359.5:c.1158T>G , LRG_318t1:c.1158T>G
|
NP_005350.1:p.Gly386=
|
|
NM_005359.6:c.1158T>G
MANE Select
|
NP_005350.1:p.Gly386=
|
|