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ENST00000576677.6:n.1490G>A
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|
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ENST00000681983.1:n.2497G>A
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|
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ENST00000682099.1:n.1258G>A
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|
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ENST00000682213.1:c.*332G>A
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ENSP00000508166.1:n.*332G>A
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ENST00000682315.1:c.675G>A
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ENSP00000507232.1:p.Leu225=
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|
ENST00000682479.1:c.2451G>A
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ENSP00000508214.1:p.Leu817=
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ENST00000682610.1:n.1601G>A
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|
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ENST00000682654.1:c.*332G>A
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ENSP00000507412.1:n.*332G>A
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ENST00000682722.1:c.2310G>A
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ENSP00000508364.1:p.Leu770=
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ENST00000683041.1:c.*332G>A
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ENSP00000506994.1:n.*332G>A
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|
ENST00000683184.1:c.*2014G>A
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ENSP00000507757.1:n.*2014G>A
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|
ENST00000683282.1:c.2277G>A
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ENSP00000506913.1:p.Leu759=
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ENST00000683444.1:c.*1938G>A
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ENSP00000507553.1:n.*1938G>A
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ENST00000683584.1:n.1184G>A
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|
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ENST00000683821.1:c.675G>A
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ENSP00000507651.1:p.Leu225=
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ENST00000683839.1:n.1815G>A
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|
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ENST00000684000.1:c.2445G>A
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ENSP00000506795.1:p.Leu815=
|
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ENST00000684188.1:c.2172G>A
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ENSP00000507153.1:p.Leu724=
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ENST00000684349.1:c.2547G>A
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ENSP00000508067.1:p.Leu849=
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ENST00000684361.1:c.2361G>A
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ENSP00000507364.1:p.Leu787=
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|
ENST00000684408.1:c.2004G>A
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ENSP00000506837.1:p.Leu668=
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|
ENST00000684429.1:c.2289G>A
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ENSP00000507224.1:p.Leu763=
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|
ENST00000684464.1:c.2454G>A
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ENSP00000508333.1:p.Leu818=
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ENST00000684544.1:c.2280G>A
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ENSP00000507337.1:p.Leu760=
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ENST00000684559.1:n.1116G>A
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|
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ENST00000684760.1:c.2628G>A
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ENSP00000507696.1:p.Leu876=
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ENST00000684776.1:c.*844G>A
|
ENSP00000507861.1:n.*844G>A
|
|
ENST00000355528.9:c.2361G>A
MANE Select
|
ENSP00000347719.4:p.Leu787=
|
|
ENST00000355528.8:c.2361G>A
|
ENSP00000347719.4:p.Leu787=
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ENST00000539345.6:c.2361G>A
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ENSP00000440671.2:p.Leu787=
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|
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ENST00000571796.5:n.1019G>A
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|
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ENST00000574422.1:c.675G>A
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ENSP00000458599.1:p.Leu225=
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ENST00000574818.5:n.419G>A
|
|
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ENST00000574886.1:n.745G>A
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|
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ENST00000574975.5:c.738G>A
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ENSP00000461680.1:p.Leu246=
|
|
ENST00000576760.5:c.675G>A
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ENSP00000460949.1:p.Leu225=
|
|
NM_005993.4:c.2361G>A
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NP_005984.3:p.Leu787=
|
|
XM_005256396.3:c.2310G>A
|
XP_005256453.1:p.Leu770=
|
|
XM_005256399.3:c.1077G>A
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XP_005256456.1:p.Leu359=
|
|
XM_005256400.3:c.675G>A
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XP_005256457.1:p.Leu225=
|
|
XM_005256401.3:c.675G>A
|
XP_005256458.1:p.Leu225=
|
|
XM_005256402.3:c.675G>A
|
XP_005256459.1:p.Leu225=
|
|
XM_005256403.3:c.675G>A
|
XP_005256460.1:p.Leu225=
|
|
XM_005256404.3:c.675G>A
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XP_005256461.1:p.Leu225=
|
|
XM_006722290.2:c.2280G>A
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XP_006722353.1:p.Leu760=
|
|
XM_006722291.2:c.1065G>A
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XP_006722354.1:p.Leu355=
|
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XM_006722292.2:c.675G>A
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XP_006722355.1:p.Leu225=
|
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XM_011523589.1:c.2016G>A
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XP_011521891.1:p.Leu672=
|
|
XM_011523590.1:c.2004G>A
|
XP_011521892.1:p.Leu668=
|
|
XM_011523591.1:c.2001G>A
|
XP_011521893.1:p.Leu667=
|
|
XM_011523592.1:c.1914G>A
|
XP_011521894.1:p.Leu638=
|
|
XM_011523593.1:c.1608G>A
|
XP_011521895.1:p.Leu536=
|
|
XM_011523594.1:c.1089G>A
|
XP_011521896.1:p.Leu363=
|
|
XM_011523595.1:c.1056G>A
|
XP_011521897.1:p.Leu352=
|
|
XM_011523597.1:c.822G>A
|
XP_011521899.1:p.Leu274=
|
|
XM_011523598.1:c.819G>A
|
XP_011521900.1:p.Leu273=
|
|
XM_011523599.1:c.813G>A
|
XP_011521901.1:p.Leu271=
|
|
XM_011523600.1:c.675G>A
|
XP_011521902.1:p.Leu225=
|
|
XR_430033.2:n.2469G>A
|
|
|
XM_005256396.4:c.2310G>A
|
XP_005256453.1:p.Leu770=
|
|
XM_005256399.5:c.1077G>A
|
XP_005256456.1:p.Leu359=
|
|
XM_005256404.4:c.675G>A
|
XP_005256461.1:p.Leu225=
|
|
XM_006722291.4:c.1065G>A
|
XP_006722354.1:p.Leu355=
|
|
XM_006722292.3:c.675G>A
|
XP_006722355.1:p.Leu225=
|
|
XM_011523589.2:c.2016G>A
|
XP_011521891.1:p.Leu672=
|
|
XM_011523591.2:c.2001G>A
|
XP_011521893.1:p.Leu667=
|
|
XM_011523593.2:c.1608G>A
|
XP_011521895.1:p.Leu536=
|
|
XM_011523594.2:c.1089G>A
|
XP_011521896.1:p.Leu363=
|
|
XM_011523595.3:c.1056G>A
|
XP_011521897.1:p.Leu352=
|
|
XM_011523597.2:c.822G>A
|
XP_011521899.1:p.Leu274=
|
|
XM_011523599.2:c.813G>A
|
XP_011521901.1:p.Leu271=
|
|
XM_011523600.3:c.675G>A
|
XP_011521902.1:p.Leu225=
|
|
XM_017024987.1:c.2172G>A
|
XP_016880476.1:p.Leu724=
|
|
XM_017024989.1:c.723G>A
|
XP_016880478.1:p.Leu241=
|
|
XM_017024990.2:c.675G>A
|
XP_016880479.1:p.Leu225=
|
|
XM_024450899.1:c.675G>A
|
XP_024306667.1:p.Leu225=
|
|
XM_024450900.1:c.675G>A
|
XP_024306668.1:p.Leu225=
|
|
XM_024450901.1:c.675G>A
|
XP_024306669.1:p.Leu225=
|
|
XM_024450902.1:c.675G>A
|
XP_024306670.1:p.Leu225=
|
|
XR_001752597.1:n.2469G>A
|
|
|
XR_001752598.1:n.2469G>A
|
|
|
XR_001752599.1:n.2469G>A
|
|
|
XR_001752600.1:n.2387G>A
|
|
|
NM_005993.5:c.2361G>A
MANE Select
|
NP_005984.3:p.Leu787=
|
|