ENST00000691309.1:c.1352-14117G>T
(CYP51A1)
|
ENSP00000510368.1:n.1352-14117G>T
|
|
ENST00000356239.8:c.10746C>A
(AKAP9)
MANE Select
|
ENSP00000348573.3:p.Gly3582=
|
|
ENST00000359028.7:c.10818C>A
(AKAP9)
|
ENSP00000351922.4:p.Gly3606=
|
|
ENST00000394534.7:c.3738C>A
(AKAP9)
|
ENSP00000378042.3:p.Gly1246=
|
|
ENST00000463118.2:n.94C>A
(AKAP9)
|
|
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ENST00000486313.2:c.234C>A
(AKAP9)
|
ENSP00000505389.1:p.Gly78=
|
|
ENST00000487692.2:n.2824C>A
(AKAP9)
|
|
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ENST00000491695.2:c.5391C>A
(AKAP9)
|
ENSP00000494626.2:p.Gly1797=
|
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ENST00000679448.1:c.*1626C>A
(AKAP9)
|
ENSP00000505889.1:n.*1626C>A
|
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ENST00000679457.1:c.10722C>A
(AKAP9)
|
ENSP00000505450.1:p.Gly3574=
|
|
ENST00000679474.1:n.10944C>A
(AKAP9)
|
|
|
ENST00000679521.1:c.10692C>A
(AKAP9)
|
ENSP00000505456.1:p.Gly3564=
|
|
ENST00000679821.1:c.10488C>A
(AKAP9)
|
ENSP00000506040.1:p.Gly3496=
|
|
ENST00000680047.1:n.12416C>A
(AKAP9)
|
|
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ENST00000680072.1:c.10569C>A
(AKAP9)
|
ENSP00000506581.1:p.Gly3523=
|
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ENST00000680181.1:c.10653C>A
(AKAP9)
|
ENSP00000505548.1:p.Gly3551=
|
|
ENST00000680365.1:c.4385C>A
(AKAP9)
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ENSP00000506019.1:n.4385C>A
|
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ENST00000680513.1:c.10605C>A
(AKAP9)
|
ENSP00000505284.1:p.Gly3535=
|
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ENST00000680534.1:c.10785C>A
(AKAP9)
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ENSP00000506674.1:p.Gly3595=
|
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ENST00000680766.1:c.10722C>A
(AKAP9)
|
ENSP00000505204.1:p.Gly3574=
|
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ENST00000680952.1:c.10722C>A
(AKAP9)
|
ENSP00000506407.1:p.Gly3574=
|
|
ENST00000681216.1:c.4506C>A
(AKAP9)
|
ENSP00000505551.1:n.4506C>A
|
|
ENST00000681412.1:c.10746C>A
(AKAP9)
|
ENSP00000506486.1:p.Gly3582=
|
|
ENST00000681722.1:c.10722C>A
(AKAP9)
|
ENSP00000506566.1:p.Gly3574=
|
|
ENST00000356239.7:c.10746C>A
(AKAP9)
|
ENSP00000348573.3:p.Gly3582=
|
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ENST00000359028.6:c.10755C>A
(AKAP9)
|
ENSP00000351922.3:p.Gly3585=
|
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ENST00000394534.6:c.4284C>A
(AKAP9)
|
ENSP00000378042.2:p.Gly1428=
|
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ENST00000463118.1:n.94C>A
(AKAP9)
|
|
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ENST00000487258.5:n.2496C>A
(AKAP9)
|
|
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ENST00000487692.1:n.546C>A
(AKAP9)
|
|
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NM_005751.4:c.10746C>A , LRG_331t1:c.10746C>A
(AKAP9)
|
NP_005742.4:p.Gly3582=
|
|
NM_147185.2:c.10722C>A
(AKAP9)
|
NP_671714.1:p.Gly3574=
|
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XM_006715827.1:c.10605C>A
(AKAP9)
|
XP_006715890.1:p.Gly3535=
|
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XM_011515709.1:c.10893C>A
(AKAP9)
|
XP_011514011.1:p.Gly3631=
|
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XM_011515710.1:c.10917C>A
(AKAP9)
|
XP_011514012.1:p.Gly3639=
|
|
XM_011515711.1:c.10857C>A
(AKAP9)
|
XP_011514013.1:p.Gly3619=
|
|
XM_011515712.1:c.10854C>A
(AKAP9)
|
XP_011514014.1:p.Gly3618=
|
|
XM_011515713.1:c.10839C>A
(AKAP9)
|
XP_011514015.1:p.Gly3613=
|
|
XM_011515714.1:c.10878C>A
(AKAP9)
|
XP_011514016.1:p.Gly3626=
|
|
XM_011515716.1:c.10797C>A
(AKAP9)
|
XP_011514018.1:p.Gly3599=
|
|
XM_011515717.1:c.10752C>A
(AKAP9)
|
XP_011514019.1:p.Gly3584=
|
|
XM_011515718.1:c.10782C>A
(AKAP9)
|
XP_011514020.1:p.Gly3594=
|
|
XM_011515719.1:c.10758C>A
(AKAP9)
|
XP_011514021.1:p.Gly3586=
|
|
XM_011515721.1:c.5406C>A
(AKAP9)
|
XP_011514023.1:p.Gly1802=
|
|
XM_011515722.1:c.5367C>A
(AKAP9)
|
XP_011514024.1:p.Gly1789=
|
|
XM_017011642.2:c.10881C>A
(AKAP9)
|
XP_016867131.1:p.Gly3627=
|
|
XM_017011643.2:c.10842C>A
(AKAP9)
|
XP_016867132.1:p.Gly3614=
|
|
XM_017011644.2:c.10881C>A
(AKAP9)
|
XP_016867133.1:p.Gly3627=
|
|
XM_017011645.2:c.10827C>A
(AKAP9)
|
XP_016867134.1:p.Gly3609=
|
|
XM_017011646.2:c.10842C>A
(AKAP9)
|
XP_016867135.1:p.Gly3614=
|
|
XM_017011647.2:c.10788C>A
(AKAP9)
|
XP_016867136.1:p.Gly3596=
|
|
XM_017011648.2:c.10785C>A
(AKAP9)
|
XP_016867137.1:p.Gly3595=
|
|
XM_017011649.2:c.10818C>A
(AKAP9)
|
XP_016867138.1:p.Gly3606=
|
|
XM_017011650.2:c.10746C>A
(AKAP9)
|
XP_016867139.1:p.Gly3582=
|
|
XM_017011651.2:c.10740C>A
(AKAP9)
|
XP_016867140.1:p.Gly3580=
|
|
XM_017011652.2:c.10692C>A
(AKAP9)
|
XP_016867141.1:p.Gly3564=
|
|
XM_017011653.2:c.10653C>A
(AKAP9)
|
XP_016867142.1:p.Gly3551=
|
|
XM_017011654.2:c.10605C>A
(AKAP9)
|
XP_016867143.1:p.Gly3535=
|
|
XM_017011655.2:c.10509C>A
(AKAP9)
|
XP_016867144.1:p.Gly3503=
|
|
XM_017011656.2:c.10509C>A
(AKAP9)
|
XP_016867145.1:p.Gly3503=
|
|
XM_017011657.2:c.6546C>A
(AKAP9)
|
XP_016867146.1:p.Gly2182=
|
|
XM_017011658.2:c.5430C>A
(AKAP9)
|
XP_016867147.1:p.Gly1810=
|
|
XM_017011659.2:c.5391C>A
(AKAP9)
|
XP_016867148.1:p.Gly1797=
|
|
XM_017011660.2:c.5391C>A
(AKAP9)
|
XP_016867149.1:p.Gly1797=
|
|
XM_024446631.1:c.10644C>A
(AKAP9)
|
XP_024302399.1:p.Gly3548=
|
|
NM_147185.3:c.10722C>A
(AKAP9)
|
NP_671714.1:p.Gly3574=
|
|
NM_001379277.1:c.5391C>A
(AKAP9)
|
NP_001366206.1:p.Gly1797=
|
|
NM_005751.5:c.10746C>A
(AKAP9)
MANE Select
|
NP_005742.4:p.Gly3582=
|
|