ENST00000366548.8:c.2508A>C
MANE Select
|
ENSP00000355506.3:p.Glu836Asp
|
|
ENST00000348581.9:c.2508A>C
|
ENSP00000311873.5:p.Glu836Asp
|
|
ENST00000366548.7:c.2508A>C
|
ENSP00000355506.3:p.Glu836Asp
|
|
ENST00000518483.5:c.*94A>C
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ENSP00000430251.1:n.*94A>C
|
|
ENST00000518741.1:n.152-2957A>C
|
|
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ENST00000521202.2:c.601A>C
|
|
|
NM_003686.4:c.*94A>C
|
NP_003677.4:n.*94A>C
|
|
NM_006027.4:c.2508A>C
|
NP_006018.4:p.Glu836Asp
|
|
NM_130398.3:c.2508A>C
|
NP_569082.2:p.Glu836Asp
|
|
XM_005273350.2:c.2505A>C
|
XP_005273407.1:p.Glu835Asp
|
|
XM_006711840.1:c.2508A>C
|
XP_006711903.1:p.Glu836Asp
|
|
XM_011544321.1:c.2508A>C
|
XP_011542623.1:p.Glu836Asp
|
|
XM_011544322.1:c.2508A>C
|
XP_011542624.1:p.Glu836Asp
|
|
XM_011544323.1:c.2505A>C
|
XP_011542625.1:p.Glu835Asp
|
|
XM_011544324.1:c.2388A>C
|
XP_011542626.1:p.Glu796Asp
|
|
XM_011544325.1:c.1545A>C
|
XP_011542627.1:p.Glu515Asp
|
|
XR_949162.1:n.2990+4060A>C
|
|
|
NM_001319224.1:c.2505A>C
|
NP_001306153.1:p.Glu835Asp
|
|
XM_006711840.2:c.2508A>C
|
XP_006711903.1:p.Glu836Asp
|
|
XM_011544321.2:c.2508A>C
|
XP_011542623.1:p.Glu836Asp
|
|
XM_011544323.2:c.2505A>C
|
XP_011542625.1:p.Glu835Asp
|
|
XM_011544324.2:c.2388A>C
|
XP_011542626.1:p.Glu796Asp
|
|
XM_011544325.2:c.1545A>C
|
XP_011542627.1:p.Glu515Asp
|
|
XM_017002793.2:c.2388A>C
|
XP_016858282.1:p.Glu796Asp
|
|
NM_130398.4:c.2508A>C
MANE Select
|
NP_569082.2:p.Glu836Asp
|
|
NM_001319224.2:c.2505A>C
|
NP_001306153.1:p.Glu835Asp
|
|