ENST00000269980.7:c.1027T>A
MANE Select
|
ENSP00000269980.2:p.Ser343Thr
|
|
ENST00000269980.6:c.1027T>A
|
ENSP00000269980.2:p.Ser343Thr
|
|
ENST00000457836.6:c.1036T>A
|
ENSP00000416000.2:p.Ser346Thr
|
|
ENST00000540732.3:c.1129T>A
|
ENSP00000443246.1:p.Ser377Thr
|
|
ENST00000542943.5:c.940T>A
|
ENSP00000440345.1:p.Ser314Thr
|
|
ENST00000595085.5:c.922+332T>A
|
ENSP00000471150.2:n.922+332T>A
|
|
NM_000709.3:c.1027T>A
|
NP_000700.1:p.Ser343Thr
|
|
NM_001164783.1:c.1024T>A
|
NP_001158255.1:p.Ser342Thr
|
|
NM_000709.4:c.1027T>A
MANE Select
|
NP_000700.1:p.Ser343Thr
|
|
NM_001164783.2:c.1024T>A
|
NP_001158255.1:p.Ser342Thr
|
|