ENST00000682565.1:c.11733G>A
|
ENSP00000507671.1:p.Gln3911=
|
|
ENST00000682801.1:c.11167-749G>A
|
ENSP00000507862.1:n.11167-749G>A
|
|
ENST00000682859.1:c.11733G>A
|
ENSP00000508222.1:p.Gln3911=
|
|
ENST00000683791.1:c.4819G>A
|
|
|
ENST00000684460.1:c.9014G>A
|
|
|
ENST00000684548.1:c.11733G>A
|
ENSP00000507421.1:p.Gln3911=
|
|
ENST00000684590.1:c.6180G>A
|
ENSP00000507376.1:p.Gln2060=
|
|
ENST00000684656.1:c.9198G>A
|
|
|
ENST00000613296.6:c.12114G>A
MANE Select
|
ENSP00000482968.1:p.Gln4038=
|
|
ENST00000651057.1:c.2268G>A
|
ENSP00000498504.1:p.Gln756=
|
|
ENST00000651434.1:c.3470G>A
|
|
|
ENST00000651750.1:c.1260+555G>A
|
|
|
ENST00000652487.1:c.3285G>A
|
|
|
ENST00000464408.3:n.289G>A
|
|
|
ENST00000484298.5:c.11988G>A
|
ENSP00000478155.1:p.Gln3996=
|
|
ENST00000613296.4:c.12114G>A
|
ENSP00000482968.1:p.Gln4038=
|
|
ENST00000620466.4:n.5917G>A
|
|
|
NM_015120.4:c.12117G>A , LRG_741t1:c.12117G>A
|
NP_055935.4:p.Gln4039=
|
|
NM_001378454.1:c.12114G>A
MANE Select
|
NP_001365383.1:p.Gln4038=
|
|