ENST00000691183.1:c.*233G>T
|
ENSP00000509954.1:n.*233G>T
|
|
ENST00000378842.8:c.645G>T
MANE Select
|
ENSP00000368119.4:p.Glu215Asp
|
|
ENST00000378842.7:c.645G>T
|
ENSP00000368119.3:p.Glu215Asp
|
|
ENST00000450095.6:c.318G>T
|
ENSP00000401956.2:p.Glu106Asp
|
|
ENST00000472111.5:n.901G>T
|
|
|
ENST00000473506.6:c.*233G>T
|
ENSP00000432839.2:n.*233G>T
|
|
ENST00000473529.5:n.804G>T
|
|
|
ENST00000487381.5:n.1030G>T
|
|
|
ENST00000489643.6:n.420G>T
|
|
|
ENST00000554085.5:c.*389G>T
|
ENSP00000450419.1:n.*389G>T
|
|
ENST00000554550.5:c.*265G>T
|
ENSP00000451435.1:n.*265G>T
|
|
ENST00000554638.5:n.1117G>T
|
|
|
ENST00000555020.5:n.801G>T
|
|
|
ENST00000555086.5:n.649G>T
|
|
|
ENST00000555214.5:n.466G>T
|
|
|
ENST00000556244.1:c.632G>T
|
|
|
ENST00000556278.1:c.390G>T
|
ENSP00000451792.1:p.Glu130Asp
|
|
ENST00000556494.5:n.766G>T
|
|
|
ENST00000557706.5:n.1207G>T
|
|
|
NM_000155.3:c.645G>T
|
NP_000146.2:p.Glu215Asp
|
|
NM_001258332.1:c.318G>T
|
NP_001245261.1:p.Glu106Asp
|
|
NM_000155.4:c.645G>T
MANE Select
|
NP_000146.2:p.Glu215Asp
|
|
NM_001258332.2:c.318G>T
|
NP_001245261.1:p.Glu106Asp
|
|