ENST00000356392.9:c.894A>C
MANE Select
|
ENSP00000348757.3:p.Glu298Asp
|
|
ENST00000356392.8:c.894A>C
|
ENSP00000348757.3:p.Glu298Asp
|
|
ENST00000586836.5:c.321A>C
|
ENSP00000467429.1:p.Glu107Asp
|
|
ENST00000591179.5:c.714A>C
|
ENSP00000466800.1:p.Glu238Asp
|
|
ENST00000591345.5:c.*813A>C
|
ENSP00000467313.1:n.*813A>C
|
|
NM_001302453.1:c.732A>C
|
NP_001289382.1:p.Glu244Asp
|
|
NM_001302454.1:c.714A>C
|
NP_001289383.1:p.Glu238Asp
|
|
NM_145045.4:c.894A>C
|
NP_659482.3:p.Glu298Asp
|
|
XM_017026241.1:c.894A>C
|
XP_016881730.1:p.Glu298Asp
|
|
NM_145045.5:c.894A>C
MANE Select
|
NP_659482.3:p.Glu298Asp
|
|
NM_001302454.2:c.714A>C
|
NP_001289383.1:p.Glu238Asp
|
|