ENST00000682565.1:c.10116A=
|
ENSP00000507671.1:p.Glu3372=
|
|
ENST00000682801.1:c.10116A=
|
ENSP00000507862.1:p.Glu3372=
|
|
ENST00000682859.1:c.10116A=
|
ENSP00000508222.1:p.Glu3372=
|
|
ENST00000683791.1:c.3202A=
|
|
|
ENST00000684460.1:c.7397A=
|
|
|
ENST00000684548.1:c.10116A=
|
ENSP00000507421.1:p.Glu3372=
|
|
ENST00000684590.1:c.4563A=
|
ENSP00000507376.1:p.Glu1521=
|
|
ENST00000684656.1:c.7442A=
|
|
|
ENST00000613296.6:c.10497A=
MANE Select
|
ENSP00000482968.1:p.Glu3499=
|
|
ENST00000651057.1:c.651A=
|
ENSP00000498504.1:p.Glu217=
|
|
ENST00000651434.1:c.1853A=
|
|
|
ENST00000652487.1:c.1594A=
|
|
|
ENST00000423048.5:c.3988A=
|
ENSP00000399833.1:n.3988A=
|
|
ENST00000484298.5:c.10371A=
|
ENSP00000478155.1:p.Glu3457=
|
|
ENST00000613296.4:c.10497A=
|
ENSP00000482968.1:p.Glu3499=
|
|
ENST00000614410.4:c.10497A=
|
ENSP00000479094.1:p.Glu3499=
|
|
ENST00000620466.4:n.4300A=
|
|
|
NM_015120.4:c.10500A= , LRG_741t1:c.10500A=
|
NP_055935.4:p.Glu3500=
|
|
NM_001378454.1:c.10497A=
MANE Select
|
NP_001365383.1:p.Glu3499=
|
|