ENST00000673918.2:c.4965C>G
|
ENSP00000501283.1:p.Asp1655Glu
|
|
ENST00000674114.2:c.2572C>G
|
ENSP00000501039.2:n.2572C>G
|
|
ENST00000684977.1:c.249C>G
|
ENSP00000509384.1:p.Asp83Glu
|
|
ENST00000685168.1:c.457C>G
|
|
|
ENST00000689544.1:n.184C>G
|
|
|
ENST00000691421.1:c.252C>G
|
ENSP00000508674.1:p.Asp84Glu
|
|
ENST00000691855.1:c.4573C>G
|
|
|
ENST00000692961.1:c.5031C>G
|
ENSP00000509289.1:p.Asp1677Glu
|
|
ENST00000420124.4:c.5031C>G
MANE Select
|
ENSP00000398837.2:p.Asp1677Glu
|
|
ENST00000673918.1:c.4965C>G
|
ENSP00000501283.1:p.Asp1655Glu
|
|
ENST00000674114.1:c.2353C>G
|
|
|
ENST00000420124.2:c.5031C>G
|
ENSP00000398837.1:p.Asp1677Glu
|
|
NM_014727.2:c.5031C>G
|
NP_055542.1:p.Asp1677Glu
|
|
XM_011527561.1:c.4965C>G
|
XP_011525863.1:p.Asp1655Glu
|
|
XM_011527562.1:c.5031C>G
|
XP_011525864.1:p.Asp1677Glu
|
|
XM_011527563.1:c.4755C>G
|
XP_011525865.1:p.Asp1585Glu
|
|
XM_011527561.2:c.4467C>G
|
XP_011525863.2:p.Asp1489Glu
|
|
XM_011527562.2:c.5031C>G
|
XP_011525864.1:p.Asp1677Glu
|
|
XM_017027544.1:c.5031C>G
|
XP_016883033.1:p.Asp1677Glu
|
|
XM_017027545.1:c.4467C>G
|
XP_016883034.1:p.Asp1489Glu
|
|
XM_017027546.1:c.1995C>G
|
XP_016883035.1:p.Asp665Glu
|
|
NM_014727.3:c.5031C>G
MANE Select
|
NP_055542.1:p.Asp1677Glu
|
|