ENST00000321264.9:c.1424A>T
MANE Select
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ENSP00000315351.4:p.Glu475Val
|
|
ENST00000321264.8:c.1424A>T
|
ENSP00000315351.4:p.Glu475Val
|
|
ENST00000400769.6:c.*174A>T
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ENSP00000383580.2:n.*174A>T
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|
ENST00000403782.5:c.1022A>T
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ENSP00000384723.1:p.Glu341Val
|
|
ENST00000436747.5:c.*2660A>T
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ENSP00000400212.1:n.*2660A>T
|
|
ENST00000445308.1:c.820A>T
|
|
|
ENST00000468064.5:n.1314A>T
|
|
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ENST00000470343.5:n.905A>T
|
|
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ENST00000473126.1:n.623A>T
|
|
|
ENST00000486953.5:n.1248A>T
|
|
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ENST00000610344.1:c.*268A>T
|
ENSP00000481906.1:n.*268A>T
|
|
NM_001287249.1:c.1022A>T
|
NP_001274178.1:p.Glu341Val
|
|
NM_152783.4:c.1424A>T
|
NP_689996.4:p.Glu475Val
|
|
NR_109778.1:n.1346A>T
|
|
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XM_011511734.1:c.1544A>T
|
XP_011510036.1:p.Glu515Val
|
|
XM_011511735.1:c.1502A>T
|
XP_011510037.1:p.Glu501Val
|
|
XM_011511736.1:c.1466A>T
|
XP_011510038.1:p.Glu489Val
|
|
XM_011511750.1:c.*91A>T
|
XP_011510052.1:n.*91A>T
|
|
XM_011511754.1:c.983A>T
|
XP_011510056.1:p.Glu328Val
|
|
XM_011511755.1:c.974A>T
|
XP_011510057.1:p.Glu325Val
|
|
XM_011511756.1:c.971A>T
|
XP_011510058.1:p.Glu324Val
|
|
XR_923004.1:n.2056A>T
|
|
|
XR_923007.1:n.1766A>T
|
|
|
XR_923011.1:n.1867A>T
|
|
|
NM_001352824.1:c.863A>T
|
NP_001339753.1:p.Glu288Val
|
|
XM_011511734.2:c.1544A>T
|
XP_011510036.1:p.Glu515Val
|
|
XM_011511735.2:c.1502A>T
|
XP_011510037.1:p.Glu501Val
|
|
XM_011511736.2:c.1466A>T
|
XP_011510038.1:p.Glu489Val
|
|
XM_011511750.3:c.*91A>T
|
XP_011510052.1:n.*91A>T
|
|
XM_011511756.2:c.971A>T
|
XP_011510058.1:p.Glu324Val
|
|
XM_024453102.1:c.1316A>T
|
XP_024308870.1:p.Glu439Val
|
|
XR_001738918.2:n.1798A>T
|
|
|
XR_001738919.2:n.1732A>T
|
|
|
XR_923004.3:n.2055A>T
|
|
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XR_923007.3:n.1765A>T
|
|
|
XR_923011.3:n.1866A>T
|
|
|
NM_152783.5:c.1424A>T
MANE Select
|
NP_689996.4:p.Glu475Val
|
|
NM_001287249.2:c.1022A>T
|
NP_001274178.1:p.Glu341Val
|
|
NM_001352824.2:c.863A>T
|
NP_001339753.1:p.Glu288Val
|
|
NR_109778.2:n.1295A>T
|
|
|