ENST00000682565.1:c.11686G=
|
ENSP00000507671.1:p.Glu3896=
|
|
ENST00000682801.1:c.11167-796G=
|
ENSP00000507862.1:n.11167-796G=
|
|
ENST00000682859.1:c.11686G=
|
ENSP00000508222.1:p.Glu3896=
|
|
ENST00000683791.1:c.4772G=
|
|
|
ENST00000684460.1:c.8967G=
|
|
|
ENST00000684548.1:c.11686G=
|
ENSP00000507421.1:p.Glu3896=
|
|
ENST00000684590.1:c.6133G=
|
ENSP00000507376.1:p.Glu2045=
|
|
ENST00000684656.1:c.9151G=
|
|
|
ENST00000613296.6:c.12067G=
MANE Select
|
ENSP00000482968.1:p.Glu4023=
|
|
ENST00000651057.1:c.2221G=
|
ENSP00000498504.1:p.Glu741=
|
|
ENST00000651434.1:c.3423G=
|
|
|
ENST00000651750.1:c.1260+508G=
|
|
|
ENST00000652487.1:c.3238G=
|
|
|
ENST00000464408.3:n.242G=
|
|
|
ENST00000484298.5:c.11941G=
|
ENSP00000478155.1:p.Glu3981=
|
|
ENST00000613296.4:c.12067G=
|
ENSP00000482968.1:p.Glu4023=
|
|
ENST00000620466.4:n.5870G=
|
|
|
NM_015120.4:c.12070G= , LRG_741t1:c.12070G=
|
NP_055935.4:p.Glu4024=
|
|
NM_001378454.1:c.12067G=
MANE Select
|
NP_001365383.1:p.Glu4023=
|
|