ENST00000592092.2:n.243C>A
|
|
|
ENST00000673918.2:c.5871C>A
|
ENSP00000501283.1:p.Asp1957Glu
|
|
ENST00000674114.2:c.3478C>A
|
ENSP00000501039.2:n.3478C>A
|
|
ENST00000684977.1:c.1155C>A
|
ENSP00000509384.1:p.Asp385Glu
|
|
ENST00000689544.1:n.1090C>A
|
|
|
ENST00000691421.1:c.1158C>A
|
ENSP00000508674.1:p.Asp386Glu
|
|
ENST00000691855.1:c.5479C>A
|
|
|
ENST00000692961.1:c.5937C>A
|
ENSP00000509289.1:p.Asp1979Glu
|
|
ENST00000693677.1:c.704+157C>A
|
ENSP00000509779.1:n.704+157C>A
|
|
ENST00000420124.4:c.5937C>A
MANE Select
|
ENSP00000398837.2:p.Asp1979Glu
|
|
ENST00000673918.1:c.5871C>A
|
ENSP00000501283.1:p.Asp1957Glu
|
|
ENST00000674114.1:c.3259C>A
|
|
|
ENST00000420124.2:c.5937C>A
|
ENSP00000398837.1:p.Asp1979Glu
|
|
NM_014727.2:c.5937C>A
|
NP_055542.1:p.Asp1979Glu
|
|
XM_011527561.1:c.5871C>A
|
XP_011525863.1:p.Asp1957Glu
|
|
XM_011527562.1:c.5937C>A
|
XP_011525864.1:p.Asp1979Glu
|
|
XM_011527563.1:c.5661C>A
|
XP_011525865.1:p.Asp1887Glu
|
|
XM_011527561.2:c.5373C>A
|
XP_011525863.2:p.Asp1791Glu
|
|
XM_011527562.2:c.5937C>A
|
XP_011525864.1:p.Asp1979Glu
|
|
XM_017027544.1:c.5937C>A
|
XP_016883033.1:p.Asp1979Glu
|
|
XM_017027545.1:c.5373C>A
|
XP_016883034.1:p.Asp1791Glu
|
|
XM_017027546.1:c.2901C>A
|
XP_016883035.1:p.Asp967Glu
|
|
NM_014727.3:c.5937C>A
MANE Select
|
NP_055542.1:p.Asp1979Glu
|
|