ENST00000682565.1:c.11688G>T
|
ENSP00000507671.1:p.Glu3896Asp
|
|
ENST00000682801.1:c.11167-794G>T
|
ENSP00000507862.1:n.11167-794G>T
|
|
ENST00000682859.1:c.11688G>T
|
ENSP00000508222.1:p.Glu3896Asp
|
|
ENST00000683791.1:c.4774G>T
|
|
|
ENST00000684460.1:c.8969G>T
|
|
|
ENST00000684548.1:c.11688G>T
|
ENSP00000507421.1:p.Glu3896Asp
|
|
ENST00000684590.1:c.6135G>T
|
ENSP00000507376.1:p.Glu2045Asp
|
|
ENST00000684656.1:c.9153G>T
|
|
|
ENST00000613296.6:c.12069G>T
MANE Select
|
ENSP00000482968.1:p.Glu4023Asp
|
|
ENST00000651057.1:c.2223G>T
|
ENSP00000498504.1:p.Glu741Asp
|
|
ENST00000651434.1:c.3425G>T
|
|
|
ENST00000651750.1:c.1260+510G>T
|
|
|
ENST00000652487.1:c.3240G>T
|
|
|
ENST00000464408.3:n.244G>T
|
|
|
ENST00000484298.5:c.11943G>T
|
ENSP00000478155.1:p.Glu3981Asp
|
|
ENST00000613296.4:c.12069G>T
|
ENSP00000482968.1:p.Glu4023Asp
|
|
ENST00000620466.4:n.5872G>T
|
|
|
NM_015120.4:c.12072G>T , LRG_741t1:c.12072G>T
|
NP_055935.4:p.Glu4024Asp
|
|
NM_001378454.1:c.12069G>T
MANE Select
|
NP_001365383.1:p.Glu4023Asp
|
|