ENST00000542639.6:c.507T>A
|
ENSP00000440846.1:p.Ala169=
|
|
ENST00000686683.1:c.216T>A
|
ENSP00000509063.1:p.Ala72=
|
|
ENST00000686980.1:n.1038T>A
|
|
|
ENST00000688006.1:c.507T>A
|
ENSP00000510311.1:p.Ala169=
|
|
ENST00000688859.1:n.462T>A
|
|
|
ENST00000689087.1:c.507T>A
|
ENSP00000508997.1:p.Ala169=
|
|
ENST00000693128.1:c.801T>A
|
ENSP00000508493.1:p.Ala267=
|
|
ENST00000338702.4:c.906T>A
MANE Select
|
ENSP00000340684.3:p.Ala302=
|
|
ENST00000338702.3:c.906T>A
|
ENSP00000340684.3:p.Ala302=
|
|
ENST00000542639.5:c.507T>A
|
ENSP00000440846.1:p.Ala169=
|
|
NM_000240.3:c.906T>A
|
NP_000231.1:p.Ala302=
|
|
NM_001270458.1:c.507T>A
|
NP_001257387.1:p.Ala169=
|
|
NM_000240.4:c.906T>A
MANE Select
|
NP_000231.1:p.Ala302=
|
|
NM_001270458.2:c.507T>A
|
NP_001257387.1:p.Ala169=
|
|