ENST00000691183.1:c.328+96G=
|
ENSP00000509954.1:n.328+96G=
|
|
ENST00000378842.8:c.335G=
MANE Select
|
ENSP00000368119.4:p.Ser112=
|
|
ENST00000378842.7:c.335G=
|
ENSP00000368119.3:p.Ser112=
|
|
ENST00000450095.6:c.51-169G=
|
ENSP00000401956.2:n.51-169G=
|
|
ENST00000465543.6:n.674G=
|
|
|
ENST00000472111.5:n.465G=
|
|
|
ENST00000473506.6:c.286G=
|
ENSP00000432839.2:p.Val96=
|
|
ENST00000473529.5:n.471G=
|
|
|
ENST00000485531.1:n.650G=
|
|
|
ENST00000487381.5:n.594G=
|
|
|
ENST00000489643.6:n.282+405G=
|
|
|
ENST00000554085.5:c.*79G=
|
ENSP00000450419.1:n.*79G=
|
|
ENST00000554139.5:n.388G=
|
|
|
ENST00000554330.5:n.372G=
|
|
|
ENST00000554550.5:c.253-169G=
|
ENSP00000451435.1:n.253-169G=
|
|
ENST00000554638.5:n.681G=
|
|
|
ENST00000554897.5:c.253-169G=
|
ENSP00000450942.1:n.253-169G=
|
|
ENST00000554944.5:n.405G=
|
|
|
ENST00000555020.5:n.365G=
|
|
|
ENST00000555086.5:n.339G=
|
|
|
ENST00000555214.5:n.262-385G=
|
|
|
ENST00000556157.1:n.459G=
|
|
|
ENST00000556244.1:c.322G=
|
|
|
ENST00000556278.1:c.252+405G=
|
ENSP00000451792.1:n.252+405G=
|
|
ENST00000556403.5:n.437G=
|
|
|
ENST00000556494.5:n.456G=
|
|
|
ENST00000557541.5:n.479G=
|
|
|
ENST00000557706.5:n.771G=
|
|
|
NM_000155.3:c.335G=
|
NP_000146.2:p.Ser112=
|
|
NM_001258332.1:c.51-169G=
|
NP_001245261.1:n.51-169G=
|
|
NM_000155.4:c.335G=
MANE Select
|
NP_000146.2:p.Ser112=
|
|
NM_001258332.2:c.51-169G=
|
NP_001245261.1:n.51-169G=
|
|