ENST00000682565.1:c.10608G>C
|
ENSP00000507671.1:p.Trp3536Cys
|
|
ENST00000682801.1:c.10608G>C
|
ENSP00000507862.1:p.Trp3536Cys
|
|
ENST00000682859.1:c.10608G>C
|
ENSP00000508222.1:p.Trp3536Cys
|
|
ENST00000683791.1:c.3694G>C
|
|
|
ENST00000684460.1:c.7889G>C
|
|
|
ENST00000684548.1:c.10608G>C
|
ENSP00000507421.1:p.Trp3536Cys
|
|
ENST00000684590.1:c.5055G>C
|
ENSP00000507376.1:p.Trp1685Cys
|
|
ENST00000684656.1:c.7934G>C
|
|
|
ENST00000613296.6:c.10989G>C
MANE Select
|
ENSP00000482968.1:p.Trp3663Cys
|
|
ENST00000651057.1:c.1143G>C
|
ENSP00000498504.1:p.Trp381Cys
|
|
ENST00000651434.1:c.2345G>C
|
|
|
ENST00000651750.1:c.377G>C
|
|
|
ENST00000652487.1:c.2086G>C
|
|
|
ENST00000423048.5:c.4480G>C
|
ENSP00000399833.1:n.4480G>C
|
|
ENST00000484298.5:c.10863G>C
|
ENSP00000478155.1:p.Trp3621Cys
|
|
ENST00000613296.4:c.10989G>C
|
ENSP00000482968.1:p.Trp3663Cys
|
|
ENST00000614410.4:c.10989G>C
|
ENSP00000479094.1:p.Trp3663Cys
|
|
ENST00000620466.4:n.4792G>C
|
|
|
NM_015120.4:c.10992G>C , LRG_741t1:c.10992G>C
|
NP_055935.4:p.Trp3664Cys
|
|
NM_001378454.1:c.10989G>C
MANE Select
|
NP_001365383.1:p.Trp3663Cys
|
|