ENST00000261304.7:c.1536T>A
MANE Select
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ENSP00000261304.2:p.Gly512=
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ENST00000261304.6:c.1536T>A
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ENSP00000261304.2:p.Gly512=
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ENST00000393568.8:c.1467T>A
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ENSP00000377198.4:p.Gly489=
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ENST00000393569.6:c.1458T>A
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ENSP00000377199.2:p.Gly486=
|
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ENST00000544807.6:c.1368T>A
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ENSP00000437513.2:p.Gly456=
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ENST00000555000.5:c.903T>A
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ENSP00000450472.1:p.Gly301=
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ENST00000555179.1:c.206+2041T>A
|
|
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ENST00000557316.5:c.*934T>A
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ENSP00000452314.1:n.*934T>A
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NM_000153.3:c.1536T>A
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NP_000144.2:p.Gly512=
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NM_001201401.1:c.1467T>A
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NP_001188330.1:p.Gly489=
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NM_001201402.1:c.1458T>A
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NP_001188331.1:p.Gly486=
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|
XM_011536618.1:c.1368T>A
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XP_011534920.1:p.Gly456=
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XM_011536618.2:c.1368T>A
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XP_011534920.1:p.Gly456=
|
|
NM_000153.4:c.1536T>A
MANE Select
|
NP_000144.2:p.Gly512=
|
|
NM_001201401.2:c.1467T>A
|
NP_001188330.1:p.Gly489=
|
|
NM_001201402.2:c.1458T>A
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NP_001188331.1:p.Gly486=
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