ENST00000691183.1:c.*233G=
|
ENSP00000509954.1:n.*233G=
|
|
ENST00000378842.8:c.645G=
MANE Select
|
ENSP00000368119.4:p.Glu215=
|
|
ENST00000378842.7:c.645G=
|
ENSP00000368119.3:p.Glu215=
|
|
ENST00000450095.6:c.318G=
|
ENSP00000401956.2:p.Glu106=
|
|
ENST00000472111.5:n.901G=
|
|
|
ENST00000473506.6:c.*233G=
|
ENSP00000432839.2:n.*233G=
|
|
ENST00000473529.5:n.804G=
|
|
|
ENST00000487381.5:n.1030G=
|
|
|
ENST00000489643.6:n.420G=
|
|
|
ENST00000554085.5:c.*389G=
|
ENSP00000450419.1:n.*389G=
|
|
ENST00000554550.5:c.*265G=
|
ENSP00000451435.1:n.*265G=
|
|
ENST00000554638.5:n.1117G=
|
|
|
ENST00000555020.5:n.801G=
|
|
|
ENST00000555086.5:n.649G=
|
|
|
ENST00000555214.5:n.466G=
|
|
|
ENST00000556244.1:c.632G=
|
|
|
ENST00000556278.1:c.390G=
|
ENSP00000451792.1:p.Glu130=
|
|
ENST00000556494.5:n.766G=
|
|
|
ENST00000557706.5:n.1207G=
|
|
|
NM_000155.3:c.645G=
|
NP_000146.2:p.Glu215=
|
|
NM_001258332.1:c.318G=
|
NP_001245261.1:p.Glu106=
|
|
NM_000155.4:c.645G=
MANE Select
|
NP_000146.2:p.Glu215=
|
|
NM_001258332.2:c.318G=
|
NP_001245261.1:p.Glu106=
|
|