ENST00000426263.10:c.359A>T
MANE Select
|
ENSP00000416293.2:p.Glu120Val
|
|
ENST00000674765.1:c.359A>T
|
ENSP00000501811.1:p.Glu120Val
|
|
ENST00000675112.1:n.382A>T
|
|
|
ENST00000676254.1:n.808A>T
|
|
|
ENST00000372500.4:c.263A>T
|
ENSP00000361578.4:p.Glu88Val
|
|
ENST00000426263.7:c.359A>T
|
ENSP00000416293.2:p.Glu120Val
|
|
ENST00000439722.2:c.238A>T
|
ENSP00000395521.2:n.238A>T
|
|
ENST00000475162.3:c.258A>T
|
|
|
ENST00000625233.2:n.567A>T
|
|
|
ENST00000630287.2:c.359A>T
|
ENSP00000486694.1:p.Glu120Val
|
|
NM_006516.2:c.359A>T
|
NP_006507.2:p.Glu120Val
|
|
NM_006516.3:c.359A>T
|
NP_006507.2:p.Glu120Val
|
|
NM_006516.4:c.359A>T
MANE Select
|
NP_006507.2:p.Glu120Val
|
|