ENST00000322213.9:c.2004G>C
MANE Select
|
ENSP00000323421.3:p.Glu668Asp
|
|
ENST00000674590.1:c.1236G>C
|
ENSP00000502626.1:p.Glu412Asp
|
|
ENST00000675065.1:n.1356G>C
|
|
|
ENST00000675504.1:c.1938G>C
|
ENSP00000502524.1:p.Glu646Asp
|
|
ENST00000322213.8:c.2004G>C
|
ENSP00000323421.3:p.Glu668Asp
|
|
ENST00000375340.10:c.1938G>C
|
ENSP00000364489.7:p.Glu646Asp
|
|
NM_001281463.1:c.1938G>C , LRG_773t1:c.1938G>C
|
NP_001268392.1:p.Glu646Asp
|
|
NM_006306.3:c.2004G>C , LRG_773t2:c.2004G>C
|
NP_006297.2:p.Glu668Asp
|
|
NM_006306.4:c.2004G>C
MANE Select
|
NP_006297.2:p.Glu668Asp
|
|