ENST00000265594.9:c.1556A>T
MANE Select
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ENSP00000265594.4:p.Glu519Val
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ENST00000265594.8:c.1556A>T
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ENSP00000265594.4:p.Glu519Val
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ENST00000476176.5:c.1415A>T
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ENSP00000420433.1:p.Glu472Val
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ENST00000489909.1:n.100A>T
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|
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ENST00000492597.5:c.1229A>T
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ENSP00000419898.1:p.Glu410Val
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ENST00000495767.5:c.*1137A>T
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ENSP00000419658.1:n.*1137A>T
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ENST00000497830.5:c.*1153A>T
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ENSP00000420088.1:n.*1153A>T
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ENST00000497959.5:c.1263+1770A>T
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ENSP00000420648.1:n.1263+1770A>T
|
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ENST00000539926.5:c.1106A>T
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ENSP00000441253.2:p.Glu369Val
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ENST00000610757.4:c.1106A>T
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ENSP00000480435.1:p.Glu369Val
|
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ENST00000629669.2:c.1263+1770A>T
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ENSP00000486824.1:n.1263+1770A>T
|
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NM_001293273.1:c.1205A>T
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NP_001280202.1:p.Glu402Val
|
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NM_020166.4:c.1556A>T
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NP_064551.3:p.Glu519Val
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NR_120639.1:n.1470A>T
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NR_120640.1:n.2044+1770A>T
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|
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XM_006713702.1:c.1229A>T
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XP_006713765.1:p.Glu410Val
|
|
XM_011512992.1:c.1442A>T
|
XP_011511294.1:p.Glu481Val
|
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XM_011512993.1:c.1377+1770A>T
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XP_011511295.1:n.1377+1770A>T
|
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XR_241502.2:n.1524+1770A>T
|
|
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XR_924159.1:n.1703A>T
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|
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NM_001363880.1:c.1229A>T
|
NP_001350809.1:p.Glu410Val
|
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XM_011512992.2:c.1442A>T
|
XP_011511294.1:p.Glu481Val
|
|
XR_001740207.2:n.1679A>T
|
|
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XR_001740208.2:n.1679A>T
|
|
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XR_001740209.2:n.1470+1770A>T
|
|
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XR_001740210.1:n.1509A>T
|
|
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XR_002959553.1:n.1679A>T
|
|
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XR_002959554.1:n.1500+1770A>T
|
|
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XR_241502.3:n.1470+1770A>T
|
|
|
NM_020166.5:c.1556A>T
MANE Select
|
NP_064551.3:p.Glu519Val
|
|
NM_001293273.2:c.1205A>T
|
NP_001280202.1:p.Glu402Val
|
|
NR_120639.2:n.1379A>T
|
|
|
NR_120640.2:n.2044+1770A>T
|
|
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