ENST00000297289.9:c.378T>G
|
ENSP00000516619.1:p.Thr126=
|
|
ENST00000418964.2:c.1476T>G
|
ENSP00000389424.2:p.Thr492=
|
|
ENST00000706906.1:c.1425T>G
|
ENSP00000516618.1:p.Thr475=
|
|
ENST00000308192.14:c.1425T>G
MANE Select
|
ENSP00000308938.9:p.Thr475=
|
|
ENST00000297289.8:n.423T>G
|
|
|
ENST00000308192.13:c.1425T>G
|
ENSP00000308938.9:p.Thr475=
|
|
ENST00000493435.1:n.480T>G
|
|
|
NM_000301.3:c.1425T>G , LRG_571t1:c.1425T>G
|
NP_000292.1:p.Thr475=
|
|
NM_000301.4:c.1425T>G
|
NP_000292.1:p.Thr475=
|
|
NM_000301.5:c.1425T>G
MANE Select
|
NP_000292.1:p.Thr475=
|
|