ENST00000375687.10:c.4062A>C
MANE Select
|
ENSP00000364839.4:p.Glu1354Asp
|
|
ENST00000646985.1:c.3879A>C
|
ENSP00000495053.1:p.Glu1293Asp
|
|
ENST00000647223.1:n.6415A>C
|
|
|
ENST00000651418.1:c.1870-1656A>C
|
ENSP00000499150.1:n.1870-1656A>C
|
|
ENST00000306058.9:c.4047A>C
|
ENSP00000305119.5:p.Glu1349Asp
|
|
ENST00000375687.8:c.4062A>C
|
ENSP00000364839.4:p.Glu1354Asp
|
|
ENST00000613218.4:c.4062A>C
|
ENSP00000480487.1:p.Glu1354Asp
|
|
ENST00000620121.4:c.4062A>C
|
ENSP00000481978.1:p.Glu1354Asp
|
|
NM_015338.5:c.4062A>C , LRG_630t1:c.4062A>C
|
NP_056153.2:p.Glu1354Asp
|
|
XM_006723727.2:c.4059A>C
|
XP_006723790.1:p.Glu1353Asp
|
|
XM_006723728.2:c.4032A>C
|
XP_006723791.1:p.Glu1344Asp
|
|
XM_006723730.2:c.3978A>C
|
XP_006723793.1:p.Glu1326Asp
|
|
XM_006723732.2:c.3879A>C
|
XP_006723795.1:p.Glu1293Asp
|
|
XM_006723733.1:c.3378A>C
|
XP_006723796.1:p.Glu1126Asp
|
|
XM_011528647.1:c.4326A>C
|
XP_011526949.1:p.Glu1442Asp
|
|
XM_011528648.1:c.4323A>C
|
XP_011526950.1:p.Glu1441Asp
|
|
XM_011528649.1:c.4242A>C
|
XP_011526951.1:p.Glu1414Asp
|
|
XM_011528650.1:c.4173A>C
|
XP_011526952.1:p.Glu1391Asp
|
|
XM_011528651.1:c.4041A>C
|
XP_011526953.1:p.Glu1347Asp
|
|
XM_011528652.1:c.3978A>C
|
XP_011526954.1:p.Glu1326Asp
|
|
NM_001363734.1:c.3879A>C
|
NP_001350663.1:p.Glu1293Asp
|
|
XM_006723727.3:c.4059A>C
|
XP_006723790.1:p.Glu1353Asp
|
|
XM_006723728.3:c.4032A>C
|
XP_006723791.1:p.Glu1344Asp
|
|
XM_006723730.4:c.3978A>C
|
XP_006723793.1:p.Glu1326Asp
|
|
XM_011528648.3:c.4323A>C
|
XP_011526950.1:p.Glu1441Asp
|
|
XM_011528652.2:c.3978A>C
|
XP_011526954.1:p.Glu1326Asp
|
|
XM_017027704.1:c.3978A>C
|
XP_016883193.1:p.Glu1326Asp
|
|
XM_017027705.1:c.3978A>C
|
XP_016883194.1:p.Glu1326Asp
|
|
XM_017027706.1:c.3909A>C
|
XP_016883195.1:p.Glu1303Asp
|
|
NM_015338.6:c.4062A>C
MANE Select
|
NP_056153.2:p.Glu1354Asp
|
|