ENST00000373327.5:c.1872G>T
MANE Select
|
ENSP00000362424.4:p.Glu624Asp
|
|
ENST00000373327.4:c.1872G>T
|
ENSP00000362424.4:p.Glu624Asp
|
|
ENST00000391993.7:c.1674G>T
|
ENSP00000375851.3:p.Glu558Asp
|
|
ENST00000462122.1:n.883G>T
|
|
|
ENST00000483951.1:n.220G>T
|
|
|
NM_001139490.1:c.1674G>T
|
NP_001132962.1:p.Glu558Asp
|
|
NM_015650.3:c.1872G>T
|
NP_056465.2:p.Glu624Asp
|
|
XM_006712414.1:c.1671G>T
|
XP_006712477.1:p.Glu557Asp
|
|
XM_011510944.1:c.1974G>T
|
XP_011509246.1:p.Glu658Asp
|
|
XM_011510945.1:c.1935G>T
|
XP_011509247.1:p.Glu645Asp
|
|
XM_011510946.1:c.1902G>T
|
XP_011509248.1:p.Glu634Asp
|
|
XM_011510947.1:c.1842G>T
|
XP_011509249.1:p.Glu614Asp
|
|
XM_011510948.1:c.1776G>T
|
XP_011509250.1:p.Glu592Asp
|
|
XM_011510950.1:c.840G>T
|
XP_011509252.1:p.Glu280Asp
|
|
XM_006712414.2:c.1671G>T
|
XP_006712477.1:p.Glu557Asp
|
|
XM_011510944.2:c.1974G>T
|
XP_011509246.1:p.Glu658Asp
|
|
XM_011510945.2:c.1935G>T
|
XP_011509247.1:p.Glu645Asp
|
|
XM_011510946.2:c.1902G>T
|
XP_011509248.1:p.Glu634Asp
|
|
XM_011510947.2:c.1842G>T
|
XP_011509249.1:p.Glu614Asp
|
|
XM_011510948.2:c.1776G>T
|
XP_011509250.1:p.Glu592Asp
|
|
XM_011510950.2:c.840G>T
|
XP_011509252.1:p.Glu280Asp
|
|
XM_017003789.1:c.1971G>T
|
XP_016859278.1:p.Glu657Asp
|
|
XR_001738696.1:n.1700G>T
|
|
|
XR_001738697.1:n.1697G>T
|
|
|
NM_015650.4:c.1872G>T
MANE Select
|
NP_056465.2:p.Glu624Asp
|
|