ENST00000691309.1:c.1352-14210A>C
(CYP51A1)
|
ENSP00000510368.1:n.1352-14210A>C
|
|
ENST00000356239.8:c.10839T>G
(AKAP9)
MANE Select
|
ENSP00000348573.3:p.Val3613=
|
|
ENST00000359028.7:c.10911T>G
(AKAP9)
|
ENSP00000351922.4:p.Val3637=
|
|
ENST00000394534.7:c.3831T>G
(AKAP9)
|
ENSP00000378042.3:p.Val1277=
|
|
ENST00000463118.2:n.187T>G
(AKAP9)
|
|
|
ENST00000486313.2:c.327T>G
(AKAP9)
|
ENSP00000505389.1:p.Val109=
|
|
ENST00000487692.2:n.2917T>G
(AKAP9)
|
|
|
ENST00000491695.2:c.5484T>G
(AKAP9)
|
ENSP00000494626.2:p.Val1828=
|
|
ENST00000679448.1:c.*1719T>G
(AKAP9)
|
ENSP00000505889.1:n.*1719T>G
|
|
ENST00000679457.1:c.10815T>G
(AKAP9)
|
ENSP00000505450.1:p.Val3605=
|
|
ENST00000679474.1:n.11037T>G
(AKAP9)
|
|
|
ENST00000679521.1:c.10785T>G
(AKAP9)
|
ENSP00000505456.1:p.Val3595=
|
|
ENST00000679821.1:c.10581T>G
(AKAP9)
|
ENSP00000506040.1:p.Val3527=
|
|
ENST00000680047.1:n.12509T>G
(AKAP9)
|
|
|
ENST00000680072.1:c.10662T>G
(AKAP9)
|
ENSP00000506581.1:p.Val3554=
|
|
ENST00000680181.1:c.10746T>G
(AKAP9)
|
ENSP00000505548.1:p.Val3582=
|
|
ENST00000680365.1:c.4478T>G
(AKAP9)
|
ENSP00000506019.1:n.4478T>G
|
|
ENST00000680513.1:c.10698T>G
(AKAP9)
|
ENSP00000505284.1:p.Val3566=
|
|
ENST00000680534.1:c.10878T>G
(AKAP9)
|
ENSP00000506674.1:p.Val3626=
|
|
ENST00000680766.1:c.10815T>G
(AKAP9)
|
ENSP00000505204.1:p.Val3605=
|
|
ENST00000680952.1:c.10815T>G
(AKAP9)
|
ENSP00000506407.1:p.Val3605=
|
|
ENST00000681216.1:c.4599T>G
(AKAP9)
|
ENSP00000505551.1:n.4599T>G
|
|
ENST00000681412.1:c.10839T>G
(AKAP9)
|
ENSP00000506486.1:p.Val3613=
|
|
ENST00000681722.1:c.10815T>G
(AKAP9)
|
ENSP00000506566.1:p.Val3605=
|
|
ENST00000356239.7:c.10839T>G
(AKAP9)
|
ENSP00000348573.3:p.Val3613=
|
|
ENST00000359028.6:c.10848T>G
(AKAP9)
|
ENSP00000351922.3:p.Val3616=
|
|
ENST00000394534.6:c.4377T>G
(AKAP9)
|
ENSP00000378042.2:p.Val1459=
|
|
ENST00000463118.1:n.187T>G
(AKAP9)
|
|
|
ENST00000487258.5:n.2589T>G
(AKAP9)
|
|
|
ENST00000487692.1:n.639T>G
(AKAP9)
|
|
|
NM_005751.4:c.10839T>G , LRG_331t1:c.10839T>G
(AKAP9)
|
NP_005742.4:p.Val3613=
|
|
NM_147185.2:c.10815T>G
(AKAP9)
|
NP_671714.1:p.Val3605=
|
|
XM_006715827.1:c.10698T>G
(AKAP9)
|
XP_006715890.1:p.Val3566=
|
|
XM_011515709.1:c.10986T>G
(AKAP9)
|
XP_011514011.1:p.Val3662=
|
|
XM_011515710.1:c.11010T>G
(AKAP9)
|
XP_011514012.1:p.Val3670=
|
|
XM_011515711.1:c.10950T>G
(AKAP9)
|
XP_011514013.1:p.Val3650=
|
|
XM_011515712.1:c.10947T>G
(AKAP9)
|
XP_011514014.1:p.Val3649=
|
|
XM_011515713.1:c.10932T>G
(AKAP9)
|
XP_011514015.1:p.Val3644=
|
|
XM_011515714.1:c.10971T>G
(AKAP9)
|
XP_011514016.1:p.Val3657=
|
|
XM_011515716.1:c.10890T>G
(AKAP9)
|
XP_011514018.1:p.Val3630=
|
|
XM_011515717.1:c.10845T>G
(AKAP9)
|
XP_011514019.1:p.Val3615=
|
|
XM_011515718.1:c.10875T>G
(AKAP9)
|
XP_011514020.1:p.Val3625=
|
|
XM_011515719.1:c.10851T>G
(AKAP9)
|
XP_011514021.1:p.Val3617=
|
|
XM_011515721.1:c.5499T>G
(AKAP9)
|
XP_011514023.1:p.Val1833=
|
|
XM_011515722.1:c.5460T>G
(AKAP9)
|
XP_011514024.1:p.Val1820=
|
|
XM_017011642.2:c.10974T>G
(AKAP9)
|
XP_016867131.1:p.Val3658=
|
|
XM_017011643.2:c.10935T>G
(AKAP9)
|
XP_016867132.1:p.Val3645=
|
|
XM_017011644.2:c.10974T>G
(AKAP9)
|
XP_016867133.1:p.Val3658=
|
|
XM_017011645.2:c.10920T>G
(AKAP9)
|
XP_016867134.1:p.Val3640=
|
|
XM_017011646.2:c.10935T>G
(AKAP9)
|
XP_016867135.1:p.Val3645=
|
|
XM_017011647.2:c.10881T>G
(AKAP9)
|
XP_016867136.1:p.Val3627=
|
|
XM_017011648.2:c.10878T>G
(AKAP9)
|
XP_016867137.1:p.Val3626=
|
|
XM_017011649.2:c.10911T>G
(AKAP9)
|
XP_016867138.1:p.Val3637=
|
|
XM_017011650.2:c.10839T>G
(AKAP9)
|
XP_016867139.1:p.Val3613=
|
|
XM_017011651.2:c.10833T>G
(AKAP9)
|
XP_016867140.1:p.Val3611=
|
|
XM_017011652.2:c.10785T>G
(AKAP9)
|
XP_016867141.1:p.Val3595=
|
|
XM_017011653.2:c.10746T>G
(AKAP9)
|
XP_016867142.1:p.Val3582=
|
|
XM_017011654.2:c.10698T>G
(AKAP9)
|
XP_016867143.1:p.Val3566=
|
|
XM_017011655.2:c.10602T>G
(AKAP9)
|
XP_016867144.1:p.Val3534=
|
|
XM_017011656.2:c.10602T>G
(AKAP9)
|
XP_016867145.1:p.Val3534=
|
|
XM_017011657.2:c.6639T>G
(AKAP9)
|
XP_016867146.1:p.Val2213=
|
|
XM_017011658.2:c.5523T>G
(AKAP9)
|
XP_016867147.1:p.Val1841=
|
|
XM_017011659.2:c.5484T>G
(AKAP9)
|
XP_016867148.1:p.Val1828=
|
|
XM_017011660.2:c.5484T>G
(AKAP9)
|
XP_016867149.1:p.Val1828=
|
|
XM_024446631.1:c.10737T>G
(AKAP9)
|
XP_024302399.1:p.Val3579=
|
|
NM_147185.3:c.10815T>G
(AKAP9)
|
NP_671714.1:p.Val3605=
|
|
NM_001379277.1:c.5484T>G
(AKAP9)
|
NP_001366206.1:p.Val1828=
|
|
NM_005751.5:c.10839T>G
(AKAP9)
MANE Select
|
NP_005742.4:p.Val3613=
|
|