ENST00000673918.2:c.4860G>C
|
ENSP00000501283.1:p.Glu1620Asp
|
|
ENST00000674114.2:c.2467G>C
|
ENSP00000501039.2:n.2467G>C
|
|
ENST00000684977.1:c.144G>C
|
ENSP00000509384.1:p.Glu48Asp
|
|
ENST00000685168.1:c.352G>C
|
|
|
ENST00000689544.1:n.79G>C
|
|
|
ENST00000691421.1:c.147G>C
|
ENSP00000508674.1:p.Glu49Asp
|
|
ENST00000691855.1:c.4468G>C
|
|
|
ENST00000692961.1:c.4926G>C
|
ENSP00000509289.1:p.Glu1642Asp
|
|
ENST00000420124.4:c.4926G>C
MANE Select
|
ENSP00000398837.2:p.Glu1642Asp
|
|
ENST00000673918.1:c.4860G>C
|
ENSP00000501283.1:p.Glu1620Asp
|
|
ENST00000674114.1:c.2248G>C
|
|
|
ENST00000420124.2:c.4926G>C
|
ENSP00000398837.1:p.Glu1642Asp
|
|
NM_014727.2:c.4926G>C
|
NP_055542.1:p.Glu1642Asp
|
|
XM_011527561.1:c.4860G>C
|
XP_011525863.1:p.Glu1620Asp
|
|
XM_011527562.1:c.4926G>C
|
XP_011525864.1:p.Glu1642Asp
|
|
XM_011527563.1:c.4650G>C
|
XP_011525865.1:p.Glu1550Asp
|
|
XM_011527561.2:c.4362G>C
|
XP_011525863.2:p.Glu1454Asp
|
|
XM_011527562.2:c.4926G>C
|
XP_011525864.1:p.Glu1642Asp
|
|
XM_017027544.1:c.4926G>C
|
XP_016883033.1:p.Glu1642Asp
|
|
XM_017027545.1:c.4362G>C
|
XP_016883034.1:p.Glu1454Asp
|
|
XM_017027546.1:c.1890G>C
|
XP_016883035.1:p.Glu630Asp
|
|
NM_014727.3:c.4926G>C
MANE Select
|
NP_055542.1:p.Glu1642Asp
|
|