|
NM_000709.4:c.566G>A
MANE Select
|
NP_000700.1:p.Arg189His
|
|
ENST00000269980.7:c.566G>A
MANE Select
|
ENSP00000269980.2:p.Arg189His
|
|
NM_000709.3:c.566G>A
|
NP_000700.1:p.Arg189His
|
|
NM_001164783.1:c.566G>A
|
NP_001158255.1:p.Arg189His
|
|
NM_001164783.2:c.566G>A
|
NP_001158255.1:p.Arg189His
|
|
ENST00000269980.6:c.566G>A
|
ENSP00000269980.2:p.Arg189His
|
|
ENST00000457836.6:c.500G>A
|
ENSP00000416000.2:p.Arg167His
|
|
ENST00000535632.5:n.195G>A
|
|
|
ENST00000538423.5:n.692G>A
|
|
|
ENST00000540732.3:c.668G>A
|
ENSP00000443246.1:p.Arg223His
|
|
ENST00000541315.1:c.466G>A
|
|
|
ENST00000542943.5:c.479G>A
|
ENSP00000440345.1:p.Arg160His
|
|
ENST00000545787.1:n.194G>A
|
|
|
ENST00000595085.5:c.566G>A
|
ENSP00000471150.2:p.Arg189His
|