ENST00000542639.6:c.459G>T
|
ENSP00000440846.1:p.Glu153Asp
|
|
ENST00000686683.1:c.168G>T
|
ENSP00000509063.1:p.Glu56Asp
|
|
ENST00000686980.1:n.990G>T
|
|
|
ENST00000688006.1:c.459G>T
|
ENSP00000510311.1:p.Glu153Asp
|
|
ENST00000688859.1:n.414G>T
|
|
|
ENST00000689087.1:c.459G>T
|
ENSP00000508997.1:p.Glu153Asp
|
|
ENST00000693128.1:c.753G>T
|
ENSP00000508493.1:p.Glu251Asp
|
|
ENST00000338702.4:c.858G>T
MANE Select
|
ENSP00000340684.3:p.Glu286Asp
|
|
ENST00000338702.3:c.858G>T
|
ENSP00000340684.3:p.Glu286Asp
|
|
ENST00000542639.5:c.459G>T
|
ENSP00000440846.1:p.Glu153Asp
|
|
NM_000240.3:c.858G>T
|
NP_000231.1:p.Glu286Asp
|
|
NM_001270458.1:c.459G>T
|
NP_001257387.1:p.Glu153Asp
|
|
NM_000240.4:c.858G>T
MANE Select
|
NP_000231.1:p.Glu286Asp
|
|
NM_001270458.2:c.459G>T
|
NP_001257387.1:p.Glu153Asp
|
|