ENST00000623535.2:c.2676A>C
MANE Select
|
ENSP00000485244.1:p.Glu892Asp
|
|
ENST00000674046.1:c.2799A>C
|
ENSP00000501174.1:p.Glu933Asp
|
|
ENST00000379989.6:c.2676A>C
|
ENSP00000369325.3:p.Glu892Asp
|
|
ENST00000379996.7:c.2676A>C
|
ENSP00000369332.3:p.Glu892Asp
|
|
ENST00000623535.1:c.2676A>C
|
ENSP00000485244.1:p.Glu892Asp
|
|
NM_001037343.1:c.2676A>C
|
NP_001032420.1:p.Glu892Asp
|
|
NM_003159.2:c.2676A>C
|
NP_003150.1:p.Glu892Asp
|
|
XM_011545569.1:c.2748A>C
|
XP_011543871.1:p.Glu916Asp
|
|
XM_011545570.1:c.2667A>C
|
XP_011543872.1:p.Glu889Asp
|
|
XR_950484.1:n.3051A>C
|
|
|
NM_001323289.1:c.2676A>C
|
NP_001310218.1:p.Glu892Asp
|
|
NM_001323289.2:c.2676A>C
MANE Select
|
NP_001310218.1:p.Glu892Asp
|
|
NM_001037343.2:c.2676A>C
|
NP_001032420.1:p.Glu892Asp
|
|
NM_003159.3:c.2676A>C
|
NP_003150.1:p.Glu892Asp
|
|