ENST00000328381.10:c.771G=
MANE Select
|
ENSP00000328340.5:p.Trp257=
|
|
ENST00000324689.8:c.608G=
|
ENSP00000323693.4:p.Gly203=
|
|
ENST00000328381.9:c.771G=
|
ENSP00000328340.5:p.Trp257=
|
|
ENST00000443677.6:c.464G=
|
ENSP00000411965.2:p.Gly155=
|
|
ENST00000535306.6:c.836G=
|
ENSP00000440470.2:p.Gly279=
|
|
NM_001184992.1:c.836G=
|
NP_001171921.1:p.Gly279=
|
|
NM_032322.3:c.771G=
|
NP_115698.3:p.Trp257=
|
|
NM_197939.1:c.608G=
|
NP_922921.1:p.Gly203=
|
|
XM_005258043.3:c.228G=
|
XP_005258100.1:p.Trp76=
|
|
XM_006722138.2:c.450G=
|
XP_006722201.1:p.Trp150=
|
|
XM_017025223.1:c.228G=
|
XP_016880712.1:p.Trp76=
|
|
XM_024451000.1:c.228G=
|
XP_024306768.1:p.Trp76=
|
|
XM_024451001.1:c.228G=
|
XP_024306769.1:p.Trp76=
|
|
XR_002958076.1:n.1104G=
|
|
|
XR_002958077.1:n.1039G=
|
|
|
XR_002958078.1:n.876G=
|
|
|
NM_032322.4:c.771G=
MANE Select
|
NP_115698.3:p.Trp257=
|
|
NM_001184992.2:c.836G=
|
NP_001171921.1:p.Gly279=
|
|
NM_197939.2:c.608G=
|
NP_922921.1:p.Gly203=
|
|