ENST00000542639.6:c.537G>A
|
ENSP00000440846.1:p.Glu179=
|
|
ENST00000686683.1:c.246G>A
|
ENSP00000509063.1:p.Glu82=
|
|
ENST00000686980.1:n.1068G>A
|
|
|
ENST00000688006.1:c.537G>A
|
ENSP00000510311.1:p.Glu179=
|
|
ENST00000688859.1:n.492G>A
|
|
|
ENST00000689087.1:c.537G>A
|
ENSP00000508997.1:p.Glu179=
|
|
ENST00000693128.1:c.831G>A
|
ENSP00000508493.1:p.Glu277=
|
|
ENST00000338702.4:c.936G>A
MANE Select
|
ENSP00000340684.3:p.Glu312=
|
|
ENST00000338702.3:c.936G>A
|
ENSP00000340684.3:p.Glu312=
|
|
ENST00000542639.5:c.537G>A
|
ENSP00000440846.1:p.Glu179=
|
|
NM_000240.3:c.936G>A
|
NP_000231.1:p.Glu312=
|
|
NM_001270458.1:c.537G>A
|
NP_001257387.1:p.Glu179=
|
|
NM_000240.4:c.936G>A
MANE Select
|
NP_000231.1:p.Glu312=
|
|
NM_001270458.2:c.537G>A
|
NP_001257387.1:p.Glu179=
|
|