ENST00000682565.1:c.10485A>C
|
ENSP00000507671.1:p.Glu3495Asp
|
|
ENST00000682801.1:c.10485A>C
|
ENSP00000507862.1:p.Glu3495Asp
|
|
ENST00000682859.1:c.10485A>C
|
ENSP00000508222.1:p.Glu3495Asp
|
|
ENST00000683791.1:c.3571A>C
|
|
|
ENST00000684460.1:c.7766A>C
|
|
|
ENST00000684548.1:c.10485A>C
|
ENSP00000507421.1:p.Glu3495Asp
|
|
ENST00000684590.1:c.4932A>C
|
ENSP00000507376.1:p.Glu1644Asp
|
|
ENST00000684656.1:c.7811A>C
|
|
|
ENST00000613296.6:c.10866A>C
MANE Select
|
ENSP00000482968.1:p.Glu3622Asp
|
|
ENST00000651057.1:c.1020A>C
|
ENSP00000498504.1:p.Glu340Asp
|
|
ENST00000651434.1:c.2222A>C
|
|
|
ENST00000651750.1:c.254A>C
|
|
|
ENST00000652487.1:c.1963A>C
|
|
|
ENST00000423048.5:c.4357A>C
|
ENSP00000399833.1:n.4357A>C
|
|
ENST00000484298.5:c.10740A>C
|
ENSP00000478155.1:p.Glu3580Asp
|
|
ENST00000613296.4:c.10866A>C
|
ENSP00000482968.1:p.Glu3622Asp
|
|
ENST00000614410.4:c.10866A>C
|
ENSP00000479094.1:p.Glu3622Asp
|
|
ENST00000620466.4:n.4669A>C
|
|
|
NM_015120.4:c.10869A>C , LRG_741t1:c.10869A>C
|
NP_055935.4:p.Glu3623Asp
|
|
NM_001378454.1:c.10866A>C
MANE Select
|
NP_001365383.1:p.Glu3622Asp
|
|