ENST00000373327.5:c.1692G>C
MANE Select
|
ENSP00000362424.4:p.Glu564Asp
|
|
ENST00000373327.4:c.1692G>C
|
ENSP00000362424.4:p.Glu564Asp
|
|
ENST00000391993.7:c.1494G>C
|
ENSP00000375851.3:p.Glu498Asp
|
|
ENST00000462122.1:n.703G>C
|
|
|
ENST00000483951.1:n.40G>C
|
|
|
NM_001139490.1:c.1494G>C
|
NP_001132962.1:p.Glu498Asp
|
|
NM_015650.3:c.1692G>C
|
NP_056465.2:p.Glu564Asp
|
|
XM_006712414.1:c.1491G>C
|
XP_006712477.1:p.Glu497Asp
|
|
XM_011510944.1:c.1794G>C
|
XP_011509246.1:p.Glu598Asp
|
|
XM_011510945.1:c.1755G>C
|
XP_011509247.1:p.Glu585Asp
|
|
XM_011510946.1:c.1722G>C
|
XP_011509248.1:p.Glu574Asp
|
|
XM_011510947.1:c.1662G>C
|
XP_011509249.1:p.Glu554Asp
|
|
XM_011510948.1:c.1596G>C
|
XP_011509250.1:p.Glu532Asp
|
|
XM_011510950.1:c.660G>C
|
XP_011509252.1:p.Glu220Asp
|
|
XR_922902.1:n.1991G>C
|
|
|
XM_006712414.2:c.1491G>C
|
XP_006712477.1:p.Glu497Asp
|
|
XM_011510944.2:c.1794G>C
|
XP_011509246.1:p.Glu598Asp
|
|
XM_011510945.2:c.1755G>C
|
XP_011509247.1:p.Glu585Asp
|
|
XM_011510946.2:c.1722G>C
|
XP_011509248.1:p.Glu574Asp
|
|
XM_011510947.2:c.1662G>C
|
XP_011509249.1:p.Glu554Asp
|
|
XM_011510948.2:c.1596G>C
|
XP_011509250.1:p.Glu532Asp
|
|
XM_011510950.2:c.660G>C
|
XP_011509252.1:p.Glu220Asp
|
|
XM_017003789.1:c.1791G>C
|
XP_016859278.1:p.Glu597Asp
|
|
XR_001738696.1:n.1520G>C
|
|
|
XR_001738697.1:n.1517G>C
|
|
|
XR_922902.2:n.2054G>C
|
|
|
NM_015650.4:c.1692G>C
MANE Select
|
NP_056465.2:p.Glu564Asp
|
|