ENST00000355112.8:c.3050A>G
MANE Select
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ENSP00000347232.3:p.Glu1017Gly
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ENST00000560559.2:n.1623A>G
|
|
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ENST00000648453.1:c.3050A>G
|
ENSP00000497646.1:p.Glu1017Gly
|
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ENST00000680772.1:c.3050A>G
|
ENSP00000506117.1:p.Glu1017Gly
|
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ENST00000681142.1:c.3050A>G
|
ENSP00000506682.1:p.Glu1017Gly
|
|
ENST00000355112.7:c.3050A>G
|
ENSP00000347232.3:p.Glu1017Gly
|
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ENST00000558825.5:n.397A>G
|
|
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ENST00000559724.5:c.*1974A>G
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ENSP00000453359.1:n.*1974A>G
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ENST00000560136.5:n.1076A>G
|
|
|
ENST00000560509.5:c.3050A>G
|
ENSP00000454158.1:p.Glu1017Gly
|
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ENST00000560559.1:n.587A>G
|
|
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NM_000057.3:c.3050A>G
|
NP_000048.1:p.Glu1017Gly
|
|
NM_001287246.1:c.3050A>G
|
NP_001274175.1:p.Glu1017Gly
|
|
NM_001287247.1:c.3050A>G
|
NP_001274176.1:p.Glu1017Gly
|
|
NM_001287248.1:c.1925A>G
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NP_001274177.1:p.Glu642Gly
|
|
XM_006720632.2:c.1088A>G
|
XP_006720695.1:p.Glu363Gly
|
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XM_011521881.1:c.1736A>G
|
XP_011520183.1:p.Glu579Gly
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XM_011521881.2:c.1736A>G
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XP_011520183.1:p.Glu579Gly
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NM_000057.4:c.3050A>G
MANE Select
|
NP_000048.1:p.Glu1017Gly
|
|
NM_001287246.2:c.3050A>G
|
NP_001274175.1:p.Glu1017Gly
|
|
NM_001287247.2:c.3050A>G
|
NP_001274176.1:p.Glu1017Gly
|
|
NM_001287248.2:c.1925A>G
|
NP_001274177.1:p.Glu642Gly
|
|