ENST00000588860.6:c.1006G=
|
ENSP00000465878.2:p.Gly336=
|
|
ENST00000589076.6:c.1006G=
|
ENSP00000466934.2:p.Gly336=
|
|
ENST00000589941.2:c.1006G=
|
ENSP00000465874.2:p.Gly336=
|
|
ENST00000590061.2:c.1006G=
|
ENSP00000464772.2:p.Gly336=
|
|
ENST00000593223.2:c.1006G=
|
ENSP00000466118.2:p.Gly336=
|
|
ENST00000611848.2:c.1006G=
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ENSP00000478613.2:p.Gly336=
|
|
ENST00000684953.1:n.2378G=
|
|
|
ENST00000685090.1:n.1457G=
|
|
|
ENST00000685232.1:n.1114G=
|
|
|
ENST00000688307.1:n.257G=
|
|
|
ENST00000688574.1:n.1114G=
|
|
|
ENST00000688903.1:n.1220G=
|
|
|
ENST00000691124.1:n.2488G=
|
|
|
ENST00000342988.8:c.1006G=
MANE Select
|
ENSP00000341551.3:p.Gly336=
|
|
ENST00000342988.7:c.1006G=
|
ENSP00000341551.3:p.Gly336=
|
|
ENST00000398417.6:c.1006G=
|
ENSP00000381452.1:p.Gly336=
|
|
ENST00000588745.5:c.718G=
|
ENSP00000464901.1:p.Gly240=
|
|
ENST00000591126.5:n.3007G=
|
|
|
ENST00000592186.5:c.955+5557G=
|
ENSP00000468611.1:n.955+5557G=
|
|
ENST00000611848.1:c.206G=
|
|
|
NM_005359.5:c.1006G= , LRG_318t1:c.1006G=
|
NP_005350.1:p.Gly336=
|
|
NM_005359.6:c.1006G=
MANE Select
|
NP_005350.1:p.Gly336=
|
|