ENST00000452508.7:c.5543A>G
|
ENSP00000388058.2:p.Asp1848Gly
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ENST00000713593.1:c.*5014A>G
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ENSP00000518889.1:n.*5014A>G
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|
ENST00000278616.9:c.5543A>G
|
ENSP00000278616.4:p.Asp1848Gly
|
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ENST00000683174.1:n.7027A>G
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|
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ENST00000683524.1:n.767A>G
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|
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ENST00000684152.1:n.1257A>G
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|
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ENST00000527805.6:c.*607A>G
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ENSP00000435747.2:n.*607A>G
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|
ENST00000675595.1:c.*607A>G
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ENSP00000502563.1:n.*607A>G
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|
ENST00000675843.1:c.5543A>G
MANE Select
|
ENSP00000501606.1:p.Asp1848Gly
|
|
ENST00000278616.8:c.5543A>G
|
ENSP00000278616.4:p.Asp1848Gly
|
|
ENST00000452508.6:c.5543A>G
|
ENSP00000388058.2:p.Asp1848Gly
|
|
ENST00000524792.5:n.1758A>G
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|
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ENST00000529588.5:c.55A>G
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|
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ENST00000533690.5:n.947A>G
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|
|
NM_000051.3:c.5543A>G , LRG_135t1:c.5543A>G
|
NP_000042.3:p.Asp1848Gly
|
|
XM_005271561.3:c.5543A>G
|
XP_005271618.2:p.Asp1848Gly
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|
XM_005271562.3:c.5543A>G
|
XP_005271619.2:p.Asp1848Gly
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|
XM_006718843.2:c.5543A>G
|
XP_006718906.1:p.Asp1848Gly
|
|
XM_006718845.1:c.1499A>G
|
XP_006718908.1:p.Asp500Gly
|
|
XM_011542840.1:c.5543A>G
|
XP_011541142.1:p.Asp1848Gly
|
|
XM_011542841.1:c.5543A>G
|
XP_011541143.1:p.Asp1848Gly
|
|
XM_011542842.1:c.5378A>G
|
XP_011541144.1:p.Asp1793Gly
|
|
XM_011542843.1:c.5543A>G
|
XP_011541145.1:p.Asp1848Gly
|
|
XM_011542844.1:c.4499A>G
|
XP_011541146.1:p.Asp1500Gly
|
|
XM_011542845.1:c.4235A>G
|
XP_011541147.1:p.Asp1412Gly
|
|
XM_011542847.1:c.614A>G
|
XP_011541149.1:p.Asp205Gly
|
|
NM_001351834.1:c.5543A>G
|
NP_001338763.1:p.Asp1848Gly
|
|
XM_005271562.5:c.5543A>G
|
XP_005271619.2:p.Asp1848Gly
|
|
XM_006718843.4:c.5543A>G
|
XP_006718906.1:p.Asp1848Gly
|
|
XM_006718845.2:c.1499A>G
|
XP_006718908.1:p.Asp500Gly
|
|
XM_011542840.3:c.5543A>G
|
XP_011541142.1:p.Asp1848Gly
|
|
XM_011542842.3:c.5378A>G
|
XP_011541144.1:p.Asp1793Gly
|
|
XM_011542843.2:c.5543A>G
|
XP_011541145.1:p.Asp1848Gly
|
|
XM_011542844.3:c.4499A>G
|
XP_011541146.1:p.Asp1500Gly
|
|
XM_011542845.2:c.4235A>G
|
XP_011541147.1:p.Asp1412Gly
|
|
XM_017017789.2:c.5543A>G
|
XP_016873278.1:p.Asp1848Gly
|
|
XM_017017790.2:c.5543A>G
|
XP_016873279.1:p.Asp1848Gly
|
|
XM_017017791.1:c.5543A>G
|
XP_016873280.1:p.Asp1848Gly
|
|
XR_002957150.1:n.6143A>G
|
|
|
NM_001351834.2:c.5543A>G
|
NP_001338763.1:p.Asp1848Gly
|
|
NM_000051.4:c.5543A>G
MANE Select
|
NP_000042.3:p.Asp1848Gly
|
|