ENST00000269980.7:c.814T>A
MANE Select
|
ENSP00000269980.2:p.Ser272Thr
|
|
ENST00000269980.6:c.814T>A
|
ENSP00000269980.2:p.Ser272Thr
|
|
ENST00000457836.6:c.748T>A
|
ENSP00000416000.2:p.Ser250Thr
|
|
ENST00000535632.5:n.443T>A
|
|
|
ENST00000540732.3:c.916T>A
|
ENSP00000443246.1:p.Ser306Thr
|
|
ENST00000542943.5:c.727T>A
|
ENSP00000440345.1:p.Ser243Thr
|
|
ENST00000545787.1:n.442T>A
|
|
|
ENST00000595085.5:c.814T>A
|
ENSP00000471150.2:p.Ser272Thr
|
|
NM_000709.3:c.814T>A
|
NP_000700.1:p.Ser272Thr
|
|
NM_001164783.1:c.814T>A
|
NP_001158255.1:p.Ser272Thr
|
|
NM_000709.4:c.814T>A
MANE Select
|
NP_000700.1:p.Ser272Thr
|
|
NM_001164783.2:c.814T>A
|
NP_001158255.1:p.Ser272Thr
|
|