ENST00000328381.10:c.782C>G
MANE Select
|
ENSP00000328340.5:p.Pro261Arg
|
|
ENST00000324689.8:c.619C>G
|
ENSP00000323693.4:p.Gln207Glu
|
|
ENST00000328381.9:c.782C>G
|
ENSP00000328340.5:p.Pro261Arg
|
|
ENST00000443677.6:c.475C>G
|
ENSP00000411965.2:p.Gln159Glu
|
|
ENST00000535306.6:c.847C>G
|
ENSP00000440470.2:p.Gln283Glu
|
|
NM_001184992.1:c.847C>G
|
NP_001171921.1:p.Gln283Glu
|
|
NM_032322.3:c.782C>G
|
NP_115698.3:p.Pro261Arg
|
|
NM_197939.1:c.619C>G
|
NP_922921.1:p.Gln207Glu
|
|
XM_005258043.3:c.239C>G
|
XP_005258100.1:p.Pro80Arg
|
|
XM_006722138.2:c.461C>G
|
XP_006722201.1:p.Pro154Arg
|
|
XM_017025223.1:c.239C>G
|
XP_016880712.1:p.Pro80Arg
|
|
XM_024451000.1:c.239C>G
|
XP_024306768.1:p.Pro80Arg
|
|
XM_024451001.1:c.239C>G
|
XP_024306769.1:p.Pro80Arg
|
|
XR_002958076.1:n.1115C>G
|
|
|
XR_002958077.1:n.1050C>G
|
|
|
XR_002958078.1:n.887C>G
|
|
|
NM_032322.4:c.782C>G
MANE Select
|
NP_115698.3:p.Pro261Arg
|
|
NM_001184992.2:c.847C>G
|
NP_001171921.1:p.Gln283Glu
|
|
NM_197939.2:c.619C>G
|
NP_922921.1:p.Gln207Glu
|
|