ENST00000691183.1:c.*232A=
|
ENSP00000509954.1:n.*232A=
|
|
ENST00000378842.8:c.644A=
MANE Select
|
ENSP00000368119.4:p.Glu215=
|
|
ENST00000378842.7:c.644A=
|
ENSP00000368119.3:p.Glu215=
|
|
ENST00000450095.6:c.317A=
|
ENSP00000401956.2:p.Glu106=
|
|
ENST00000472111.5:n.900A=
|
|
|
ENST00000473506.6:c.*232A=
|
ENSP00000432839.2:n.*232A=
|
|
ENST00000473529.5:n.803A=
|
|
|
ENST00000487381.5:n.1029A=
|
|
|
ENST00000489643.6:n.419A=
|
|
|
ENST00000554085.5:c.*388A=
|
ENSP00000450419.1:n.*388A=
|
|
ENST00000554550.5:c.*264A=
|
ENSP00000451435.1:n.*264A=
|
|
ENST00000554638.5:n.1116A=
|
|
|
ENST00000555020.5:n.800A=
|
|
|
ENST00000555086.5:n.648A=
|
|
|
ENST00000555214.5:n.465A=
|
|
|
ENST00000556244.1:c.631A=
|
|
|
ENST00000556278.1:c.389A=
|
ENSP00000451792.1:p.Glu130=
|
|
ENST00000556494.5:n.765A=
|
|
|
ENST00000557706.5:n.1206A=
|
|
|
NM_000155.3:c.644A=
|
NP_000146.2:p.Glu215=
|
|
NM_001258332.1:c.317A=
|
NP_001245261.1:p.Glu106=
|
|
NM_000155.4:c.644A=
MANE Select
|
NP_000146.2:p.Glu215=
|
|
NM_001258332.2:c.317A=
|
NP_001245261.1:p.Glu106=
|
|