ENST00000682565.1:c.11681G>A
|
ENSP00000507671.1:p.Gly3894Asp
|
|
ENST00000682801.1:c.11167-801G>A
|
ENSP00000507862.1:n.11167-801G>A
|
|
ENST00000682859.1:c.11681G>A
|
ENSP00000508222.1:p.Gly3894Asp
|
|
ENST00000683791.1:c.4767G>A
|
|
|
ENST00000684460.1:c.8962G>A
|
|
|
ENST00000684548.1:c.11681G>A
|
ENSP00000507421.1:p.Gly3894Asp
|
|
ENST00000684590.1:c.6128G>A
|
ENSP00000507376.1:p.Gly2043Asp
|
|
ENST00000684656.1:c.9146G>A
|
|
|
ENST00000613296.6:c.12062G>A
MANE Select
|
ENSP00000482968.1:p.Gly4021Asp
|
|
ENST00000651057.1:c.2216G>A
|
ENSP00000498504.1:p.Gly739Asp
|
|
ENST00000651434.1:c.3418G>A
|
|
|
ENST00000651750.1:c.1260+503G>A
|
|
|
ENST00000652487.1:c.3233G>A
|
|
|
ENST00000464408.3:n.237G>A
|
|
|
ENST00000484298.5:c.11936G>A
|
ENSP00000478155.1:p.Gly3979Asp
|
|
ENST00000613296.4:c.12062G>A
|
ENSP00000482968.1:p.Gly4021Asp
|
|
ENST00000620466.4:n.5865G>A
|
|
|
NM_015120.4:c.12065G>A , LRG_741t1:c.12065G>A
|
NP_055935.4:p.Gly4022Asp
|
|
NM_001378454.1:c.12062G>A
MANE Select
|
NP_001365383.1:p.Gly4021Asp
|
|