ENST00000691183.1:c.328+97T=
|
ENSP00000509954.1:n.328+97T=
|
|
ENST00000378842.8:c.336T=
MANE Select
|
ENSP00000368119.4:p.Ser112=
|
|
ENST00000378842.7:c.336T=
|
ENSP00000368119.3:p.Ser112=
|
|
ENST00000450095.6:c.51-168T=
|
ENSP00000401956.2:n.51-168T=
|
|
ENST00000465543.6:n.675T=
|
|
|
ENST00000472111.5:n.466T=
|
|
|
ENST00000473506.6:c.287T=
|
ENSP00000432839.2:p.Val96=
|
|
ENST00000473529.5:n.472T=
|
|
|
ENST00000485531.1:n.651T=
|
|
|
ENST00000487381.5:n.595T=
|
|
|
ENST00000489643.6:n.282+406T=
|
|
|
ENST00000554085.5:c.*80T=
|
ENSP00000450419.1:n.*80T=
|
|
ENST00000554139.5:n.389T=
|
|
|
ENST00000554330.5:n.373T=
|
|
|
ENST00000554550.5:c.253-168T=
|
ENSP00000451435.1:n.253-168T=
|
|
ENST00000554638.5:n.682T=
|
|
|
ENST00000554897.5:c.253-168T=
|
ENSP00000450942.1:n.253-168T=
|
|
ENST00000554944.5:n.406T=
|
|
|
ENST00000555020.5:n.366T=
|
|
|
ENST00000555086.5:n.340T=
|
|
|
ENST00000555214.5:n.262-384T=
|
|
|
ENST00000556157.1:n.460T=
|
|
|
ENST00000556244.1:c.323T=
|
|
|
ENST00000556278.1:c.252+406T=
|
ENSP00000451792.1:n.252+406T=
|
|
ENST00000556403.5:n.438T=
|
|
|
ENST00000556494.5:n.457T=
|
|
|
ENST00000557541.5:n.480T=
|
|
|
ENST00000557706.5:n.772T=
|
|
|
NM_000155.3:c.336T=
|
NP_000146.2:p.Ser112=
|
|
NM_001258332.1:c.51-168T=
|
NP_001245261.1:n.51-168T=
|
|
NM_000155.4:c.336T=
MANE Select
|
NP_000146.2:p.Ser112=
|
|
NM_001258332.2:c.51-168T=
|
NP_001245261.1:n.51-168T=
|
|