ENST00000280326.9:c.348G>A
MANE Select
|
ENSP00000280326.4:p.Leu116=
|
|
ENST00000280326.8:c.348G>A
|
ENSP00000280326.4:p.Leu116=
|
|
ENST00000423695.6:n.128-2140G>A
|
|
|
ENST00000503026.5:c.285G>A
|
ENSP00000423318.1:p.Leu95=
|
|
ENST00000503454.5:c.237G>A
|
|
|
ENST00000506600.1:c.69G>A
|
ENSP00000423052.1:p.Leu23=
|
|
ENST00000511700.1:c.263G>A
|
ENSP00000423087.1:p.Cys88Tyr
|
|
ENST00000512975.5:c.106-2140G>A
|
ENSP00000425751.1:n.106-2140G>A
|
|
ENST00000515390.5:c.183G>A
|
ENSP00000426923.1:p.Leu61=
|
|
ENST00000515676.5:c.234G>A
|
ENSP00000427297.1:p.Leu78=
|
|
ENST00000625723.1:c.106-2140G>A
|
ENSP00000487128.1:n.106-2140G>A
|
|
NM_001306153.1:c.285G>A
|
NP_001293082.1:p.Leu95=
|
|
NM_001306154.1:c.183G>A
|
NP_001293083.1:p.Leu61=
|
|
NM_001306155.1:c.69G>A
|
NP_001293084.1:p.Leu23=
|
|
NM_001306156.1:c.234G>A
|
NP_001293085.1:p.Leu78=
|
|
NM_012073.3:c.348G>A , LRG_361t1:c.348G>A
|
NP_036205.1:p.Leu116=
|
|
NM_012073.4:c.348G>A
|
NP_036205.1:p.Leu116=
|
|
NM_012073.5:c.348G>A
MANE Select
|
NP_036205.1:p.Leu116=
|
|
NM_001306154.2:c.183G>A
|
NP_001293083.1:p.Leu61=
|
|
NM_001306155.2:c.69G>A
|
NP_001293084.1:p.Leu23=
|
|
NM_001306156.2:c.234G>A
|
NP_001293085.1:p.Leu78=
|
|