ENST00000682565.1:c.10542A>C
|
ENSP00000507671.1:p.Thr3514=
|
|
ENST00000682801.1:c.10542A>C
|
ENSP00000507862.1:p.Thr3514=
|
|
ENST00000682859.1:c.10542A>C
|
ENSP00000508222.1:p.Thr3514=
|
|
ENST00000683791.1:c.3628A>C
|
|
|
ENST00000684460.1:c.7823A>C
|
|
|
ENST00000684548.1:c.10542A>C
|
ENSP00000507421.1:p.Thr3514=
|
|
ENST00000684590.1:c.4989A>C
|
ENSP00000507376.1:p.Thr1663=
|
|
ENST00000684656.1:c.7868A>C
|
|
|
ENST00000613296.6:c.10923A>C
MANE Select
|
ENSP00000482968.1:p.Thr3641=
|
|
ENST00000651057.1:c.1077A>C
|
ENSP00000498504.1:p.Thr359=
|
|
ENST00000651434.1:c.2279A>C
|
|
|
ENST00000651750.1:c.311A>C
|
|
|
ENST00000652487.1:c.2020A>C
|
|
|
ENST00000423048.5:c.4414A>C
|
ENSP00000399833.1:n.4414A>C
|
|
ENST00000484298.5:c.10797A>C
|
ENSP00000478155.1:p.Thr3599=
|
|
ENST00000613296.4:c.10923A>C
|
ENSP00000482968.1:p.Thr3641=
|
|
ENST00000614410.4:c.10923A>C
|
ENSP00000479094.1:p.Thr3641=
|
|
ENST00000620466.4:n.4726A>C
|
|
|
NM_015120.4:c.10926A>C , LRG_741t1:c.10926A>C
|
NP_055935.4:p.Thr3642=
|
|
NM_001378454.1:c.10923A>C
MANE Select
|
NP_001365383.1:p.Thr3641=
|
|