ENST00000691183.1:c.*193A>T
|
ENSP00000509954.1:n.*193A>T
|
|
ENST00000378842.8:c.605A>T
MANE Select
|
ENSP00000368119.4:p.Glu202Val
|
|
ENST00000378842.7:c.605A>T
|
ENSP00000368119.3:p.Glu202Val
|
|
ENST00000450095.6:c.278A>T
|
ENSP00000401956.2:p.Glu93Val
|
|
ENST00000472111.5:n.861A>T
|
|
|
ENST00000473506.6:c.*193A>T
|
ENSP00000432839.2:n.*193A>T
|
|
ENST00000473529.5:n.764A>T
|
|
|
ENST00000485531.1:n.1199A>T
|
|
|
ENST00000487381.5:n.990A>T
|
|
|
ENST00000489643.6:n.380A>T
|
|
|
ENST00000554085.5:c.*349A>T
|
ENSP00000450419.1:n.*349A>T
|
|
ENST00000554139.5:n.851A>T
|
|
|
ENST00000554550.5:c.*225A>T
|
ENSP00000451435.1:n.*225A>T
|
|
ENST00000554638.5:n.1077A>T
|
|
|
ENST00000554897.5:c.*292A>T
|
ENSP00000450942.1:n.*292A>T
|
|
ENST00000554944.5:n.954A>T
|
|
|
ENST00000555020.5:n.761A>T
|
|
|
ENST00000555086.5:n.609A>T
|
|
|
ENST00000555214.5:n.426A>T
|
|
|
ENST00000556244.1:c.592A>T
|
|
|
ENST00000556278.1:c.350A>T
|
ENSP00000451792.1:p.Glu117Val
|
|
ENST00000556494.5:n.726A>T
|
|
|
ENST00000557706.5:n.1167A>T
|
|
|
NM_000155.3:c.605A>T
|
NP_000146.2:p.Glu202Val
|
|
NM_001258332.1:c.278A>T
|
NP_001245261.1:p.Glu93Val
|
|
NM_000155.4:c.605A>T
MANE Select
|
NP_000146.2:p.Glu202Val
|
|
NM_001258332.2:c.278A>T
|
NP_001245261.1:p.Glu93Val
|
|