ENST00000682565.1:c.11545A>G
|
ENSP00000507671.1:p.Asn3849Asp
|
|
ENST00000682801.1:c.11167-937A>G
|
ENSP00000507862.1:n.11167-937A>G
|
|
ENST00000682859.1:c.11545A>G
|
ENSP00000508222.1:p.Asn3849Asp
|
|
ENST00000683791.1:c.4631A>G
|
|
|
ENST00000684460.1:c.8826A>G
|
|
|
ENST00000684548.1:c.11545A>G
|
ENSP00000507421.1:p.Asn3849Asp
|
|
ENST00000684590.1:c.5992A>G
|
ENSP00000507376.1:p.Asn1998Asp
|
|
ENST00000684656.1:c.9010A>G
|
|
|
ENST00000613296.6:c.11926A>G
MANE Select
|
ENSP00000482968.1:p.Asn3976Asp
|
|
ENST00000651057.1:c.2080A>G
|
ENSP00000498504.1:p.Asn694Asp
|
|
ENST00000651434.1:c.3282A>G
|
|
|
ENST00000651750.1:c.1260+367A>G
|
|
|
ENST00000652487.1:c.3097A>G
|
|
|
ENST00000464408.3:n.101A>G
|
|
|
ENST00000484298.5:c.11800A>G
|
ENSP00000478155.1:p.Asn3934Asp
|
|
ENST00000613296.4:c.11926A>G
|
ENSP00000482968.1:p.Asn3976Asp
|
|
ENST00000620466.4:n.5729A>G
|
|
|
NM_015120.4:c.11929A>G , LRG_741t1:c.11929A>G
|
NP_055935.4:p.Asn3977Asp
|
|
NM_001378454.1:c.11926A>G
MANE Select
|
NP_001365383.1:p.Asn3976Asp
|
|