ENST00000321264.9:c.1093G>T
MANE Select
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ENSP00000315351.4:p.Gly365Cys
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ENST00000321264.8:c.1093G>T
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ENSP00000315351.4:p.Gly365Cys
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ENST00000400769.6:c.854-4508G>T
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ENSP00000383580.2:n.854-4508G>T
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ENST00000403782.5:c.691G>T
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ENSP00000384723.1:p.Gly231Cys
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ENST00000432449.1:c.353G>T
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ENST00000436747.5:c.*1409G>T
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ENSP00000400212.1:n.*1409G>T
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ENST00000454048.1:c.196G>T
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ENSP00000404596.1:p.Gly66Cys
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ENST00000467427.5:n.389+1047G>T
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ENST00000470343.5:n.574G>T
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ENST00000473126.1:n.292G>T
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ENST00000486953.5:n.163+1047G>T
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ENST00000496252.5:n.448G>T
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NM_001287249.1:c.691G>T
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NP_001274178.1:p.Gly231Cys
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NM_152783.4:c.1093G>T
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NP_689996.4:p.Gly365Cys
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NR_109778.1:n.1063-4508G>T
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XM_011511734.1:c.1171G>T
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XP_011510036.1:p.Gly391Cys
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XM_011511735.1:c.1171G>T
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XP_011510037.1:p.Gly391Cys
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|
XM_011511736.1:c.1093G>T
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XP_011510038.1:p.Gly365Cys
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XM_011511737.1:c.1171G>T
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XP_011510039.1:p.Gly391Cys
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|
XM_011511742.1:c.1308G>T
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XP_011510044.1:p.Pro436=
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XM_011511743.1:c.1308G>T
|
XP_011510045.1:p.Pro436=
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|
XM_011511744.1:c.1308G>T
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XP_011510046.1:p.Pro436=
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XM_011511745.1:c.1171G>T
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XP_011510047.1:p.Gly391Cys
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XM_011511748.1:c.1242G>T
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XP_011510050.1:p.Pro414=
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XM_011511749.1:c.1179+1047G>T
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XP_011510051.1:n.1179+1047G>T
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XM_011511750.1:c.1171G>T
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XP_011510052.1:p.Gly391Cys
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XM_011511751.1:c.1212+762G>T
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XP_011510053.1:n.1212+762G>T
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XM_011511753.1:c.1075+1047G>T
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XP_011510055.1:n.1075+1047G>T
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XM_011511754.1:c.610G>T
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XP_011510056.1:p.Gly204Cys
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XM_011511755.1:c.601G>T
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XP_011510057.1:p.Gly201Cys
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XM_011511756.1:c.853+6464G>T
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XP_011510058.1:n.853+6464G>T
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XR_241434.3:n.1432G>T
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XR_923003.1:n.1954G>T
|
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XR_923004.1:n.1725G>T
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XR_923005.1:n.1468G>T
|
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XR_923006.1:n.1468G>T
|
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XR_923007.1:n.1435G>T
|
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XR_923008.1:n.1331G>T
|
|
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XR_923009.1:n.1331G>T
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XR_923010.1:n.1765G>T
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XR_923011.1:n.1536G>T
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XR_923012.1:n.1470G>T
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XR_923014.1:n.1014-4508G>T
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NM_001352824.1:c.532G>T
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NP_001339753.1:p.Gly178Cys
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XM_011511734.2:c.1171G>T
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XP_011510036.1:p.Gly391Cys
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XM_011511735.2:c.1171G>T
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XP_011510037.1:p.Gly391Cys
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XM_011511736.2:c.1093G>T
|
XP_011510038.1:p.Gly365Cys
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|
XM_011511737.3:c.1171G>T
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XP_011510039.1:p.Gly391Cys
|
|
XM_011511743.2:c.1308G>T
|
XP_011510045.1:p.Pro436=
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|
XM_011511744.2:c.1308G>T
|
XP_011510046.1:p.Pro436=
|
|
XM_011511745.3:c.1171G>T
|
XP_011510047.1:p.Gly391Cys
|
|
XM_011511749.3:c.1179+1047G>T
|
XP_011510051.1:n.1179+1047G>T
|
|
XM_011511750.3:c.1171G>T
|
XP_011510052.1:p.Gly391Cys
|
|
XM_011511751.2:c.1212+762G>T
|
XP_011510053.1:n.1212+762G>T
|
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XM_011511753.3:c.1075+1047G>T
|
XP_011510055.1:n.1075+1047G>T
|
|
XM_011511756.2:c.853+6464G>T
|
XP_011510058.1:n.853+6464G>T
|
|
XM_017004828.2:c.1093G>T
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XP_016860317.1:p.Gly365Cys
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XM_017004829.2:c.1308G>T
|
XP_016860318.1:p.Pro436=
|
|
XM_017004830.2:c.1171G>T
|
XP_016860319.1:p.Gly391Cys
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XM_024453102.1:c.943G>T
|
XP_024308870.1:p.Gly315Cys
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XR_001738918.2:n.1467G>T
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XR_001738919.2:n.1401G>T
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XR_002959334.1:n.1953G>T
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XR_002959335.1:n.1597G>T
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XR_241434.4:n.1431G>T
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XR_923004.3:n.1724G>T
|
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XR_923005.2:n.1467G>T
|
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XR_923007.3:n.1434G>T
|
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XR_923009.2:n.1330G>T
|
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XR_923010.2:n.1764G>T
|
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XR_923011.3:n.1535G>T
|
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XR_923012.2:n.1469G>T
|
|
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XR_923014.3:n.1013-4508G>T
|
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|
NM_152783.5:c.1093G>T
MANE Select
|
NP_689996.4:p.Gly365Cys
|
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NM_001287249.2:c.691G>T
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NP_001274178.1:p.Gly231Cys
|
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NM_001352824.2:c.532G>T
|
NP_001339753.1:p.Gly178Cys
|
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NR_109778.2:n.1012-4508G>T
|
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