ENST00000373327.5:c.1864C>G
MANE Select
|
ENSP00000362424.4:p.His622Asp
|
|
ENST00000373327.4:c.1864C>G
|
ENSP00000362424.4:p.His622Asp
|
|
ENST00000391993.7:c.1666C>G
|
ENSP00000375851.3:p.His556Asp
|
|
ENST00000462122.1:n.875C>G
|
|
|
ENST00000483951.1:n.212C>G
|
|
|
NM_001139490.1:c.1666C>G
|
NP_001132962.1:p.His556Asp
|
|
NM_015650.3:c.1864C>G
|
NP_056465.2:p.His622Asp
|
|
XM_006712414.1:c.1663C>G
|
XP_006712477.1:p.His555Asp
|
|
XM_011510944.1:c.1966C>G
|
XP_011509246.1:p.His656Asp
|
|
XM_011510945.1:c.1927C>G
|
XP_011509247.1:p.His643Asp
|
|
XM_011510946.1:c.1894C>G
|
XP_011509248.1:p.His632Asp
|
|
XM_011510947.1:c.1834C>G
|
XP_011509249.1:p.His612Asp
|
|
XM_011510948.1:c.1768C>G
|
XP_011509250.1:p.His590Asp
|
|
XM_011510950.1:c.832C>G
|
XP_011509252.1:p.His278Asp
|
|
XM_006712414.2:c.1663C>G
|
XP_006712477.1:p.His555Asp
|
|
XM_011510944.2:c.1966C>G
|
XP_011509246.1:p.His656Asp
|
|
XM_011510945.2:c.1927C>G
|
XP_011509247.1:p.His643Asp
|
|
XM_011510946.2:c.1894C>G
|
XP_011509248.1:p.His632Asp
|
|
XM_011510947.2:c.1834C>G
|
XP_011509249.1:p.His612Asp
|
|
XM_011510948.2:c.1768C>G
|
XP_011509250.1:p.His590Asp
|
|
XM_011510950.2:c.832C>G
|
XP_011509252.1:p.His278Asp
|
|
XM_017003789.1:c.1963C>G
|
XP_016859278.1:p.His655Asp
|
|
XR_001738696.1:n.1692C>G
|
|
|
XR_001738697.1:n.1689C>G
|
|
|
NM_015650.4:c.1864C>G
MANE Select
|
NP_056465.2:p.His622Asp
|
|