ENST00000691183.1:c.251A>T
|
ENSP00000509954.1:p.Glu84Val
|
|
ENST00000378842.8:c.251A>T
MANE Select
|
ENSP00000368119.4:p.Glu84Val
|
|
ENST00000378842.7:c.251A>T
|
ENSP00000368119.3:p.Glu84Val
|
|
ENST00000450095.6:c.49A>T
|
ENSP00000401956.2:p.Ser17Cys
|
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ENST00000465543.6:n.590A>T
|
|
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ENST00000468099.2:n.291A>T
|
|
|
ENST00000472111.5:n.292A>T
|
|
|
ENST00000473506.6:c.251A>T
|
ENSP00000432839.2:p.Glu84Val
|
|
ENST00000473529.5:n.298A>T
|
|
|
ENST00000485531.1:n.244A>T
|
|
|
ENST00000487381.5:n.277A>T
|
|
|
ENST00000489643.6:n.281A>T
|
|
|
ENST00000554085.5:c.251A>T
|
ENSP00000450419.1:p.Glu84Val
|
|
ENST00000554139.5:n.304A>T
|
|
|
ENST00000554330.5:n.248A>T
|
|
|
ENST00000554550.5:c.251A>T
|
ENSP00000451435.1:p.Glu84Val
|
|
ENST00000554638.5:n.275A>T
|
|
|
ENST00000554897.5:c.251A>T
|
ENSP00000450942.1:p.Glu84Val
|
|
ENST00000554944.5:n.281A>T
|
|
|
ENST00000555020.5:n.281A>T
|
|
|
ENST00000555086.5:n.255A>T
|
|
|
ENST00000555214.5:n.260A>T
|
|
|
ENST00000556157.1:n.358A>T
|
|
|
ENST00000556244.1:c.135A>T
|
|
|
ENST00000556278.1:c.251A>T
|
ENSP00000451792.1:p.Glu84Val
|
|
ENST00000556403.5:n.264A>T
|
|
|
ENST00000556494.5:n.283A>T
|
|
|
ENST00000557541.5:n.444A>T
|
|
|
ENST00000557706.5:n.365A>T
|
|
|
NM_000155.3:c.251A>T
|
NP_000146.2:p.Glu84Val
|
|
NM_001258332.1:c.49A>T
|
NP_001245261.1:p.Ser17Cys
|
|
NM_000155.4:c.251A>T
MANE Select
|
NP_000146.2:p.Glu84Val
|
|
NM_001258332.2:c.49A>T
|
NP_001245261.1:p.Ser17Cys
|
|