ENST00000691183.1:c.213C>A
|
ENSP00000509954.1:p.Leu71=
|
|
ENST00000378842.8:c.213C>A
MANE Select
|
ENSP00000368119.4:p.Leu71=
|
|
ENST00000378842.7:c.213C>A
|
ENSP00000368119.3:p.Leu71=
|
|
ENST00000450095.6:c.11C>A
|
ENSP00000401956.2:p.Ser4Ter
|
|
ENST00000465543.6:n.552C>A
|
|
|
ENST00000468099.2:n.253C>A
|
|
|
ENST00000472111.5:n.254C>A
|
|
|
ENST00000473506.6:c.213C>A
|
ENSP00000432839.2:p.Leu71=
|
|
ENST00000473529.5:n.260C>A
|
|
|
ENST00000485531.1:n.206C>A
|
|
|
ENST00000487381.5:n.239C>A
|
|
|
ENST00000489643.6:n.243C>A
|
|
|
ENST00000554085.5:c.213C>A
|
ENSP00000450419.1:p.Leu71=
|
|
ENST00000554139.5:n.266C>A
|
|
|
ENST00000554330.5:n.210C>A
|
|
|
ENST00000554550.5:c.213C>A
|
ENSP00000451435.1:p.Leu71=
|
|
ENST00000554638.5:n.237C>A
|
|
|
ENST00000554897.5:c.213C>A
|
ENSP00000450942.1:p.Leu71=
|
|
ENST00000554944.5:n.243C>A
|
|
|
ENST00000555020.5:n.243C>A
|
|
|
ENST00000555086.5:n.217C>A
|
|
|
ENST00000555214.5:n.222C>A
|
|
|
ENST00000556157.1:n.320C>A
|
|
|
ENST00000556244.1:c.97C>A
|
|
|
ENST00000556278.1:c.213C>A
|
ENSP00000451792.1:p.Leu71=
|
|
ENST00000556403.5:n.226C>A
|
|
|
ENST00000556494.5:n.245C>A
|
|
|
ENST00000557541.5:n.406C>A
|
|
|
ENST00000557706.5:n.327C>A
|
|
|
NM_000155.3:c.213C>A
|
NP_000146.2:p.Leu71=
|
|
NM_001258332.1:c.11C>A
|
NP_001245261.1:p.Ser4Ter
|
|
NM_000155.4:c.213C>A
MANE Select
|
NP_000146.2:p.Leu71=
|
|
NM_001258332.2:c.11C>A
|
NP_001245261.1:p.Ser4Ter
|
|