ENST00000269980.7:c.906T>C
MANE Select
|
ENSP00000269980.2:p.Asp302=
|
|
ENST00000269980.6:c.906T>C
|
ENSP00000269980.2:p.Asp302=
|
|
ENST00000457836.6:c.840T>C
|
ENSP00000416000.2:p.Asp280=
|
|
ENST00000535632.5:n.535T>C
|
|
|
ENST00000540732.3:c.1008T>C
|
ENSP00000443246.1:p.Asp336=
|
|
ENST00000542943.5:c.819T>C
|
ENSP00000440345.1:p.Asp273=
|
|
ENST00000545787.1:n.534T>C
|
|
|
ENST00000595085.5:c.906T>C
|
ENSP00000471150.2:p.Asp302=
|
|
NM_000709.3:c.906T>C
|
NP_000700.1:p.Asp302=
|
|
NM_001164783.1:c.903T>C
|
NP_001158255.1:p.Asp301=
|
|
NM_000709.4:c.906T>C
MANE Select
|
NP_000700.1:p.Asp302=
|
|
NM_001164783.2:c.903T>C
|
NP_001158255.1:p.Asp301=
|
|