ENST00000280326.9:c.342T=
MANE Select
|
ENSP00000280326.4:p.Gly114=
|
|
ENST00000280326.8:c.342T=
|
ENSP00000280326.4:p.Gly114=
|
|
ENST00000423695.6:n.128-2146T=
|
|
|
ENST00000503026.5:c.279T=
|
ENSP00000423318.1:p.Gly93=
|
|
ENST00000503454.5:c.231T=
|
|
|
ENST00000506600.1:c.63T=
|
ENSP00000423052.1:p.Gly21=
|
|
ENST00000511700.1:c.257T=
|
ENSP00000423087.1:p.Val86=
|
|
ENST00000512975.5:c.106-2146T=
|
ENSP00000425751.1:n.106-2146T=
|
|
ENST00000515390.5:c.177T=
|
ENSP00000426923.1:p.Gly59=
|
|
ENST00000515676.5:c.228T=
|
ENSP00000427297.1:p.Gly76=
|
|
ENST00000625723.1:c.106-2146T=
|
ENSP00000487128.1:n.106-2146T=
|
|
NM_001306153.1:c.279T=
|
NP_001293082.1:p.Gly93=
|
|
NM_001306154.1:c.177T=
|
NP_001293083.1:p.Gly59=
|
|
NM_001306155.1:c.63T=
|
NP_001293084.1:p.Gly21=
|
|
NM_001306156.1:c.228T=
|
NP_001293085.1:p.Gly76=
|
|
NM_012073.3:c.342T= , LRG_361t1:c.342T=
|
NP_036205.1:p.Gly114=
|
|
NM_012073.4:c.342T=
|
NP_036205.1:p.Gly114=
|
|
NM_012073.5:c.342T=
MANE Select
|
NP_036205.1:p.Gly114=
|
|
NM_001306154.2:c.177T=
|
NP_001293083.1:p.Gly59=
|
|
NM_001306155.2:c.63T=
|
NP_001293084.1:p.Gly21=
|
|
NM_001306156.2:c.228T=
|
NP_001293085.1:p.Gly76=
|
|