ENST00000377833.10:c.7188G>T
MANE Select
|
ENSP00000367064.4:p.Glu2396Asp
|
|
ENST00000377833.8:c.7188G>T
|
ENSP00000367064.4:p.Glu2396Asp
|
|
NM_001081.3:c.7188G>T , LRG_540t1:c.7188G>T
|
NP_001072.2:p.Glu2396Asp
|
|
XM_011519708.1:c.7188G>T
|
XP_011518010.1:p.Glu2396Asp
|
|
XM_011519709.1:c.3174G>T
|
XP_011518011.1:p.Glu1058Asp
|
|
XM_011519710.1:c.3150G>T
|
XP_011518012.1:p.Glu1050Asp
|
|
XM_011519711.1:c.3030G>T
|
XP_011518013.1:p.Glu1010Asp
|
|
XM_011519708.2:c.7188G>T
|
XP_011518010.1:p.Glu2396Asp
|
|
XM_011519709.2:c.3174G>T
|
XP_011518011.1:p.Glu1058Asp
|
|
XM_011519710.2:c.3150G>T
|
XP_011518012.1:p.Glu1050Asp
|
|
XM_011519711.3:c.3030G>T
|
XP_011518013.1:p.Glu1010Asp
|
|
NM_001081.4:c.7188G>T
MANE Select
|
NP_001072.2:p.Glu2396Asp
|
|