ENST00000373327.5:c.1707G>T
MANE Select
|
ENSP00000362424.4:p.Glu569Asp
|
|
ENST00000373327.4:c.1707G>T
|
ENSP00000362424.4:p.Glu569Asp
|
|
ENST00000391993.7:c.1509G>T
|
ENSP00000375851.3:p.Glu503Asp
|
|
ENST00000462122.1:n.718G>T
|
|
|
ENST00000483951.1:n.55G>T
|
|
|
NM_001139490.1:c.1509G>T
|
NP_001132962.1:p.Glu503Asp
|
|
NM_015650.3:c.1707G>T
|
NP_056465.2:p.Glu569Asp
|
|
XM_006712414.1:c.1506G>T
|
XP_006712477.1:p.Glu502Asp
|
|
XM_011510944.1:c.1809G>T
|
XP_011509246.1:p.Glu603Asp
|
|
XM_011510945.1:c.1770G>T
|
XP_011509247.1:p.Glu590Asp
|
|
XM_011510946.1:c.1737G>T
|
XP_011509248.1:p.Glu579Asp
|
|
XM_011510947.1:c.1677G>T
|
XP_011509249.1:p.Glu559Asp
|
|
XM_011510948.1:c.1611G>T
|
XP_011509250.1:p.Glu537Asp
|
|
XM_011510950.1:c.675G>T
|
XP_011509252.1:p.Glu225Asp
|
|
XR_922902.1:n.2006G>T
|
|
|
XM_006712414.2:c.1506G>T
|
XP_006712477.1:p.Glu502Asp
|
|
XM_011510944.2:c.1809G>T
|
XP_011509246.1:p.Glu603Asp
|
|
XM_011510945.2:c.1770G>T
|
XP_011509247.1:p.Glu590Asp
|
|
XM_011510946.2:c.1737G>T
|
XP_011509248.1:p.Glu579Asp
|
|
XM_011510947.2:c.1677G>T
|
XP_011509249.1:p.Glu559Asp
|
|
XM_011510948.2:c.1611G>T
|
XP_011509250.1:p.Glu537Asp
|
|
XM_011510950.2:c.675G>T
|
XP_011509252.1:p.Glu225Asp
|
|
XM_017003789.1:c.1806G>T
|
XP_016859278.1:p.Glu602Asp
|
|
XR_001738696.1:n.1535G>T
|
|
|
XR_001738697.1:n.1532G>T
|
|
|
XR_922902.2:n.2069G>T
|
|
|
NM_015650.4:c.1707G>T
MANE Select
|
NP_056465.2:p.Glu569Asp
|
|