ENST00000379644.9:c.1412A>T
MANE Select
|
ENSP00000368965.4:p.Glu471Val
|
|
ENST00000379644.8:c.1412A>T
|
ENSP00000368965.4:p.Glu471Val
|
|
ENST00000520678.1:n.345A>T
|
|
|
ENST00000521576.1:c.563A>T
|
ENSP00000429029.1:p.Glu188Val
|
|
ENST00000524016.5:c.516A>T
|
|
|
NM_152419.2:c.1412A>T
|
NP_689632.2:p.Glu471Val
|
|
XM_005273409.1:c.1412A>T
|
XP_005273466.1:p.Glu471Val
|
|
XM_005273410.1:c.1412A>T
|
XP_005273467.1:p.Glu471Val
|
|
XM_005273411.1:c.1220A>T
|
XP_005273468.1:p.Glu407Val
|
|
XM_005273412.2:c.1412A>T
|
XP_005273469.1:p.Glu471Val
|
|
NM_001363227.1:c.1412A>T
|
NP_001350156.1:p.Glu471Val
|
|
NM_001363228.1:c.1220A>T
|
NP_001350157.1:p.Glu407Val
|
|
NM_001363229.1:c.548A>T
|
NP_001350158.1:p.Glu183Val
|
|
XM_005273412.4:c.1412A>T
|
XP_005273469.1:p.Glu471Val
|
|
NM_152419.3:c.1412A>T
MANE Select
|
NP_689632.2:p.Glu471Val
|
|
NM_001363227.2:c.1412A>T
|
NP_001350156.1:p.Glu471Val
|
|
NM_001363228.2:c.1220A>T
|
NP_001350157.1:p.Glu407Val
|
|
NM_001363229.2:c.548A>T
|
NP_001350158.1:p.Glu183Val
|
|