ENST00000269980.7:c.713A>C
MANE Select
|
ENSP00000269980.2:p.Glu238Ala
|
|
ENST00000269980.6:c.713A>C
|
ENSP00000269980.2:p.Glu238Ala
|
|
ENST00000457836.6:c.647A>C
|
ENSP00000416000.2:p.Glu216Ala
|
|
ENST00000535632.5:n.342A>C
|
|
|
ENST00000540732.3:c.815A>C
|
ENSP00000443246.1:p.Glu272Ala
|
|
ENST00000541315.1:c.613A>C
|
|
|
ENST00000542943.5:c.626A>C
|
ENSP00000440345.1:p.Glu209Ala
|
|
ENST00000545787.1:n.341A>C
|
|
|
ENST00000595085.5:c.713A>C
|
ENSP00000471150.2:p.Glu238Ala
|
|
NM_000709.3:c.713A>C
|
NP_000700.1:p.Glu238Ala
|
|
NM_001164783.1:c.713A>C
|
NP_001158255.1:p.Glu238Ala
|
|
NM_000709.4:c.713A>C
MANE Select
|
NP_000700.1:p.Glu238Ala
|
|
NM_001164783.2:c.713A>C
|
NP_001158255.1:p.Glu238Ala
|
|