ENST00000269980.7:c.698T>C
MANE Select
|
ENSP00000269980.2:p.Ile233Thr
|
|
ENST00000269980.6:c.698T>C
|
ENSP00000269980.2:p.Ile233Thr
|
|
ENST00000457836.6:c.632T>C
|
ENSP00000416000.2:p.Ile211Thr
|
|
ENST00000535632.5:n.327T>C
|
|
|
ENST00000540732.3:c.800T>C
|
ENSP00000443246.1:p.Ile267Thr
|
|
ENST00000541315.1:c.598T>C
|
|
|
ENST00000542943.5:c.611T>C
|
ENSP00000440345.1:p.Ile204Thr
|
|
ENST00000545787.1:n.326T>C
|
|
|
ENST00000595085.5:c.698T>C
|
ENSP00000471150.2:p.Ile233Thr
|
|
NM_000709.3:c.698T>C
|
NP_000700.1:p.Ile233Thr
|
|
NM_001164783.1:c.698T>C
|
NP_001158255.1:p.Ile233Thr
|
|
NM_000709.4:c.698T>C
MANE Select
|
NP_000700.1:p.Ile233Thr
|
|
NM_001164783.2:c.698T>C
|
NP_001158255.1:p.Ile233Thr
|
|