ENST00000682565.1:c.10239A>G
|
ENSP00000507671.1:p.Thr3413=
|
|
ENST00000682801.1:c.10239A>G
|
ENSP00000507862.1:p.Thr3413=
|
|
ENST00000682859.1:c.10239A>G
|
ENSP00000508222.1:p.Thr3413=
|
|
ENST00000683791.1:c.3325A>G
|
|
|
ENST00000684460.1:c.7520A>G
|
|
|
ENST00000684548.1:c.10239A>G
|
ENSP00000507421.1:p.Thr3413=
|
|
ENST00000684590.1:c.4686A>G
|
ENSP00000507376.1:p.Thr1562=
|
|
ENST00000684656.1:c.7565A>G
|
|
|
ENST00000613296.6:c.10620A>G
MANE Select
|
ENSP00000482968.1:p.Thr3540=
|
|
ENST00000651057.1:c.774A>G
|
ENSP00000498504.1:p.Thr258=
|
|
ENST00000651434.1:c.1976A>G
|
|
|
ENST00000651750.1:c.8A>G
|
|
|
ENST00000652487.1:c.1717A>G
|
|
|
ENST00000423048.5:c.4111A>G
|
ENSP00000399833.1:n.4111A>G
|
|
ENST00000484298.5:c.10494A>G
|
ENSP00000478155.1:p.Thr3498=
|
|
ENST00000613296.4:c.10620A>G
|
ENSP00000482968.1:p.Thr3540=
|
|
ENST00000614410.4:c.10620A>G
|
ENSP00000479094.1:p.Thr3540=
|
|
ENST00000620466.4:n.4423A>G
|
|
|
NM_015120.4:c.10623A>G , LRG_741t1:c.10623A>G
|
NP_055935.4:p.Thr3541=
|
|
NM_001378454.1:c.10620A>G
MANE Select
|
NP_001365383.1:p.Thr3540=
|
|