ENST00000373327.5:c.1904A>G
MANE Select
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ENSP00000362424.4:p.Glu635Gly
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ENST00000373327.4:c.1904A>G
|
ENSP00000362424.4:p.Glu635Gly
|
|
ENST00000391993.7:c.1706A>G
|
ENSP00000375851.3:p.Glu569Gly
|
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ENST00000462122.1:n.915A>G
|
|
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ENST00000483951.1:n.252A>G
|
|
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NM_001139490.1:c.1706A>G
|
NP_001132962.1:p.Glu569Gly
|
|
NM_015650.3:c.1904A>G
|
NP_056465.2:p.Glu635Gly
|
|
XM_006712414.1:c.1703A>G
|
XP_006712477.1:p.Glu568Gly
|
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XM_011510944.1:c.2006A>G
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XP_011509246.1:p.Glu669Gly
|
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XM_011510945.1:c.1967A>G
|
XP_011509247.1:p.Glu656Gly
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|
XM_011510946.1:c.1934A>G
|
XP_011509248.1:p.Glu645Gly
|
|
XM_011510947.1:c.1874A>G
|
XP_011509249.1:p.Glu625Gly
|
|
XM_011510948.1:c.1808A>G
|
XP_011509250.1:p.Glu603Gly
|
|
XM_011510950.1:c.872A>G
|
XP_011509252.1:p.Glu291Gly
|
|
XM_006712414.2:c.1703A>G
|
XP_006712477.1:p.Glu568Gly
|
|
XM_011510944.2:c.2006A>G
|
XP_011509246.1:p.Glu669Gly
|
|
XM_011510945.2:c.1967A>G
|
XP_011509247.1:p.Glu656Gly
|
|
XM_011510946.2:c.1934A>G
|
XP_011509248.1:p.Glu645Gly
|
|
XM_011510947.2:c.1874A>G
|
XP_011509249.1:p.Glu625Gly
|
|
XM_011510948.2:c.1808A>G
|
XP_011509250.1:p.Glu603Gly
|
|
XM_011510950.2:c.872A>G
|
XP_011509252.1:p.Glu291Gly
|
|
XM_017003789.1:c.2003A>G
|
XP_016859278.1:p.Glu668Gly
|
|
XR_001738696.1:n.1732A>G
|
|
|
XR_001738697.1:n.1729A>G
|
|
|
NM_015650.4:c.1904A>G
MANE Select
|
NP_056465.2:p.Glu635Gly
|
|