ENST00000269980.7:c.788T>C
MANE Select
|
ENSP00000269980.2:p.Phe263Ser
|
|
ENST00000269980.6:c.788T>C
|
ENSP00000269980.2:p.Phe263Ser
|
|
ENST00000457836.6:c.722T>C
|
ENSP00000416000.2:p.Phe241Ser
|
|
ENST00000535632.5:n.417T>C
|
|
|
ENST00000540732.3:c.890T>C
|
ENSP00000443246.1:p.Phe297Ser
|
|
ENST00000542943.5:c.701T>C
|
ENSP00000440345.1:p.Phe234Ser
|
|
ENST00000545787.1:n.416T>C
|
|
|
ENST00000595085.5:c.788T>C
|
ENSP00000471150.2:p.Phe263Ser
|
|
NM_000709.3:c.788T>C
|
NP_000700.1:p.Phe263Ser
|
|
NM_001164783.1:c.788T>C
|
NP_001158255.1:p.Phe263Ser
|
|
NM_000709.4:c.788T>C
MANE Select
|
NP_000700.1:p.Phe263Ser
|
|
NM_001164783.2:c.788T>C
|
NP_001158255.1:p.Phe263Ser
|
|