ENST00000691183.1:c.328+109T>A
|
ENSP00000509954.1:n.328+109T>A
|
|
ENST00000378842.8:c.348T>A
MANE Select
|
ENSP00000368119.4:p.Leu116=
|
|
ENST00000378842.7:c.348T>A
|
ENSP00000368119.3:p.Leu116=
|
|
ENST00000450095.6:c.51-156T>A
|
ENSP00000401956.2:n.51-156T>A
|
|
ENST00000465543.6:n.687T>A
|
|
|
ENST00000472111.5:n.478T>A
|
|
|
ENST00000473506.6:c.299T>A
|
ENSP00000432839.2:p.Phe100Tyr
|
|
ENST00000473529.5:n.484T>A
|
|
|
ENST00000485531.1:n.663T>A
|
|
|
ENST00000487381.5:n.607T>A
|
|
|
ENST00000489643.6:n.282+418T>A
|
|
|
ENST00000554085.5:c.*92T>A
|
ENSP00000450419.1:n.*92T>A
|
|
ENST00000554139.5:n.401T>A
|
|
|
ENST00000554330.5:n.385T>A
|
|
|
ENST00000554550.5:c.253-156T>A
|
ENSP00000451435.1:n.253-156T>A
|
|
ENST00000554638.5:n.694T>A
|
|
|
ENST00000554897.5:c.253-156T>A
|
ENSP00000450942.1:n.253-156T>A
|
|
ENST00000554944.5:n.418T>A
|
|
|
ENST00000555020.5:n.378T>A
|
|
|
ENST00000555086.5:n.352T>A
|
|
|
ENST00000555214.5:n.262-372T>A
|
|
|
ENST00000556157.1:n.472T>A
|
|
|
ENST00000556244.1:c.335T>A
|
|
|
ENST00000556278.1:c.252+418T>A
|
ENSP00000451792.1:n.252+418T>A
|
|
ENST00000556403.5:n.450T>A
|
|
|
ENST00000556494.5:n.469T>A
|
|
|
ENST00000557541.5:n.492T>A
|
|
|
ENST00000557706.5:n.784T>A
|
|
|
NM_000155.3:c.348T>A
|
NP_000146.2:p.Leu116=
|
|
NM_001258332.1:c.51-156T>A
|
NP_001245261.1:n.51-156T>A
|
|
NM_000155.4:c.348T>A
MANE Select
|
NP_000146.2:p.Leu116=
|
|
NM_001258332.2:c.51-156T>A
|
NP_001245261.1:n.51-156T>A
|
|