ENST00000328381.10:c.818A>G
MANE Select
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ENSP00000328340.5:p.Glu273Gly
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ENST00000324689.8:c.*22A>G
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ENSP00000323693.4:n.*22A>G
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|
ENST00000328381.9:c.818A>G
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ENSP00000328340.5:p.Glu273Gly
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ENST00000443677.6:c.*22A>G
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ENSP00000411965.2:n.*22A>G
|
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ENST00000535306.6:c.*22A>G
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ENSP00000440470.2:n.*22A>G
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NM_001184992.1:c.*22A>G
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NP_001171921.1:n.*22A>G
|
|
NM_032322.3:c.818A>G
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NP_115698.3:p.Glu273Gly
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NM_197939.1:c.*22A>G
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NP_922921.1:n.*22A>G
|
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XM_005258043.3:c.275A>G
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XP_005258100.1:p.Glu92Gly
|
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XM_006722138.2:c.497A>G
|
XP_006722201.1:p.Glu166Gly
|
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XM_017025223.1:c.275A>G
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XP_016880712.1:p.Glu92Gly
|
|
XM_024451000.1:c.275A>G
|
XP_024306768.1:p.Glu92Gly
|
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XM_024451001.1:c.275A>G
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XP_024306769.1:p.Glu92Gly
|
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XR_002958076.1:n.1151A>G
|
|
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XR_002958077.1:n.1086A>G
|
|
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XR_002958078.1:n.923A>G
|
|
|
NM_032322.4:c.818A>G
MANE Select
|
NP_115698.3:p.Glu273Gly
|
|
NM_001184992.2:c.*22A>G
|
NP_001171921.1:n.*22A>G
|
|
NM_197939.2:c.*22A>G
|
NP_922921.1:n.*22A>G
|
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