ENST00000682565.1:c.10307C=
|
ENSP00000507671.1:p.Thr3436=
|
|
ENST00000682801.1:c.10307C=
|
ENSP00000507862.1:p.Thr3436=
|
|
ENST00000682859.1:c.10307C=
|
ENSP00000508222.1:p.Thr3436=
|
|
ENST00000683791.1:c.3393C=
|
|
|
ENST00000684460.1:c.7588C=
|
|
|
ENST00000684548.1:c.10307C=
|
ENSP00000507421.1:p.Thr3436=
|
|
ENST00000684590.1:c.4754C=
|
ENSP00000507376.1:p.Thr1585=
|
|
ENST00000684656.1:c.7633C=
|
|
|
ENST00000613296.6:c.10688C=
MANE Select
|
ENSP00000482968.1:p.Thr3563=
|
|
ENST00000651057.1:c.842C=
|
ENSP00000498504.1:p.Thr281=
|
|
ENST00000651434.1:c.2044C=
|
|
|
ENST00000651750.1:c.76C=
|
|
|
ENST00000652487.1:c.1785C=
|
|
|
ENST00000423048.5:c.4179C=
|
ENSP00000399833.1:n.4179C=
|
|
ENST00000484298.5:c.10562C=
|
ENSP00000478155.1:p.Thr3521=
|
|
ENST00000613296.4:c.10688C=
|
ENSP00000482968.1:p.Thr3563=
|
|
ENST00000614410.4:c.10688C=
|
ENSP00000479094.1:p.Thr3563=
|
|
ENST00000620466.4:n.4491C=
|
|
|
NM_015120.4:c.10691C= , LRG_741t1:c.10691C=
|
NP_055935.4:p.Thr3564=
|
|
NM_001378454.1:c.10688C=
MANE Select
|
NP_001365383.1:p.Thr3563=
|
|