ENST00000691309.1:c.1352-14126A>T
(CYP51A1)
|
ENSP00000510368.1:n.1352-14126A>T
|
|
ENST00000356239.8:c.10755T>A
(AKAP9)
MANE Select
|
ENSP00000348573.3:p.Thr3585=
|
|
ENST00000359028.7:c.10827T>A
(AKAP9)
|
ENSP00000351922.4:p.Thr3609=
|
|
ENST00000394534.7:c.3747T>A
(AKAP9)
|
ENSP00000378042.3:p.Thr1249=
|
|
ENST00000463118.2:n.103T>A
(AKAP9)
|
|
|
ENST00000486313.2:c.243T>A
(AKAP9)
|
ENSP00000505389.1:p.Thr81=
|
|
ENST00000487692.2:n.2833T>A
(AKAP9)
|
|
|
ENST00000491695.2:c.5400T>A
(AKAP9)
|
ENSP00000494626.2:p.Thr1800=
|
|
ENST00000679448.1:c.*1635T>A
(AKAP9)
|
ENSP00000505889.1:n.*1635T>A
|
|
ENST00000679457.1:c.10731T>A
(AKAP9)
|
ENSP00000505450.1:p.Thr3577=
|
|
ENST00000679474.1:n.10953T>A
(AKAP9)
|
|
|
ENST00000679521.1:c.10701T>A
(AKAP9)
|
ENSP00000505456.1:p.Thr3567=
|
|
ENST00000679821.1:c.10497T>A
(AKAP9)
|
ENSP00000506040.1:p.Thr3499=
|
|
ENST00000680047.1:n.12425T>A
(AKAP9)
|
|
|
ENST00000680072.1:c.10578T>A
(AKAP9)
|
ENSP00000506581.1:p.Thr3526=
|
|
ENST00000680181.1:c.10662T>A
(AKAP9)
|
ENSP00000505548.1:p.Thr3554=
|
|
ENST00000680365.1:c.4394T>A
(AKAP9)
|
ENSP00000506019.1:n.4394T>A
|
|
ENST00000680513.1:c.10614T>A
(AKAP9)
|
ENSP00000505284.1:p.Thr3538=
|
|
ENST00000680534.1:c.10794T>A
(AKAP9)
|
ENSP00000506674.1:p.Thr3598=
|
|
ENST00000680766.1:c.10731T>A
(AKAP9)
|
ENSP00000505204.1:p.Thr3577=
|
|
ENST00000680952.1:c.10731T>A
(AKAP9)
|
ENSP00000506407.1:p.Thr3577=
|
|
ENST00000681216.1:c.4515T>A
(AKAP9)
|
ENSP00000505551.1:n.4515T>A
|
|
ENST00000681412.1:c.10755T>A
(AKAP9)
|
ENSP00000506486.1:p.Thr3585=
|
|
ENST00000681722.1:c.10731T>A
(AKAP9)
|
ENSP00000506566.1:p.Thr3577=
|
|
ENST00000356239.7:c.10755T>A
(AKAP9)
|
ENSP00000348573.3:p.Thr3585=
|
|
ENST00000359028.6:c.10764T>A
(AKAP9)
|
ENSP00000351922.3:p.Thr3588=
|
|
ENST00000394534.6:c.4293T>A
(AKAP9)
|
ENSP00000378042.2:p.Thr1431=
|
|
ENST00000463118.1:n.103T>A
(AKAP9)
|
|
|
ENST00000487258.5:n.2505T>A
(AKAP9)
|
|
|
ENST00000487692.1:n.555T>A
(AKAP9)
|
|
|
NM_005751.4:c.10755T>A , LRG_331t1:c.10755T>A
(AKAP9)
|
NP_005742.4:p.Thr3585=
|
|
NM_147185.2:c.10731T>A
(AKAP9)
|
NP_671714.1:p.Thr3577=
|
|
XM_006715827.1:c.10614T>A
(AKAP9)
|
XP_006715890.1:p.Thr3538=
|
|
XM_011515709.1:c.10902T>A
(AKAP9)
|
XP_011514011.1:p.Thr3634=
|
|
XM_011515710.1:c.10926T>A
(AKAP9)
|
XP_011514012.1:p.Thr3642=
|
|
XM_011515711.1:c.10866T>A
(AKAP9)
|
XP_011514013.1:p.Thr3622=
|
|
XM_011515712.1:c.10863T>A
(AKAP9)
|
XP_011514014.1:p.Thr3621=
|
|
XM_011515713.1:c.10848T>A
(AKAP9)
|
XP_011514015.1:p.Thr3616=
|
|
XM_011515714.1:c.10887T>A
(AKAP9)
|
XP_011514016.1:p.Thr3629=
|
|
XM_011515716.1:c.10806T>A
(AKAP9)
|
XP_011514018.1:p.Thr3602=
|
|
XM_011515717.1:c.10761T>A
(AKAP9)
|
XP_011514019.1:p.Thr3587=
|
|
XM_011515718.1:c.10791T>A
(AKAP9)
|
XP_011514020.1:p.Thr3597=
|
|
XM_011515719.1:c.10767T>A
(AKAP9)
|
XP_011514021.1:p.Thr3589=
|
|
XM_011515721.1:c.5415T>A
(AKAP9)
|
XP_011514023.1:p.Thr1805=
|
|
XM_011515722.1:c.5376T>A
(AKAP9)
|
XP_011514024.1:p.Thr1792=
|
|
XM_017011642.2:c.10890T>A
(AKAP9)
|
XP_016867131.1:p.Thr3630=
|
|
XM_017011643.2:c.10851T>A
(AKAP9)
|
XP_016867132.1:p.Thr3617=
|
|
XM_017011644.2:c.10890T>A
(AKAP9)
|
XP_016867133.1:p.Thr3630=
|
|
XM_017011645.2:c.10836T>A
(AKAP9)
|
XP_016867134.1:p.Thr3612=
|
|
XM_017011646.2:c.10851T>A
(AKAP9)
|
XP_016867135.1:p.Thr3617=
|
|
XM_017011647.2:c.10797T>A
(AKAP9)
|
XP_016867136.1:p.Thr3599=
|
|
XM_017011648.2:c.10794T>A
(AKAP9)
|
XP_016867137.1:p.Thr3598=
|
|
XM_017011649.2:c.10827T>A
(AKAP9)
|
XP_016867138.1:p.Thr3609=
|
|
XM_017011650.2:c.10755T>A
(AKAP9)
|
XP_016867139.1:p.Thr3585=
|
|
XM_017011651.2:c.10749T>A
(AKAP9)
|
XP_016867140.1:p.Thr3583=
|
|
XM_017011652.2:c.10701T>A
(AKAP9)
|
XP_016867141.1:p.Thr3567=
|
|
XM_017011653.2:c.10662T>A
(AKAP9)
|
XP_016867142.1:p.Thr3554=
|
|
XM_017011654.2:c.10614T>A
(AKAP9)
|
XP_016867143.1:p.Thr3538=
|
|
XM_017011655.2:c.10518T>A
(AKAP9)
|
XP_016867144.1:p.Thr3506=
|
|
XM_017011656.2:c.10518T>A
(AKAP9)
|
XP_016867145.1:p.Thr3506=
|
|
XM_017011657.2:c.6555T>A
(AKAP9)
|
XP_016867146.1:p.Thr2185=
|
|
XM_017011658.2:c.5439T>A
(AKAP9)
|
XP_016867147.1:p.Thr1813=
|
|
XM_017011659.2:c.5400T>A
(AKAP9)
|
XP_016867148.1:p.Thr1800=
|
|
XM_017011660.2:c.5400T>A
(AKAP9)
|
XP_016867149.1:p.Thr1800=
|
|
XM_024446631.1:c.10653T>A
(AKAP9)
|
XP_024302399.1:p.Thr3551=
|
|
NM_147185.3:c.10731T>A
(AKAP9)
|
NP_671714.1:p.Thr3577=
|
|
NM_001379277.1:c.5400T>A
(AKAP9)
|
NP_001366206.1:p.Thr1800=
|
|
NM_005751.5:c.10755T>A
(AKAP9)
MANE Select
|
NP_005742.4:p.Thr3585=
|
|