ENST00000269980.7:c.1029A>C
MANE Select
|
ENSP00000269980.2:p.Ser343=
|
|
ENST00000269980.6:c.1029A>C
|
ENSP00000269980.2:p.Ser343=
|
|
ENST00000457836.6:c.1038A>C
|
ENSP00000416000.2:p.Ser346=
|
|
ENST00000540732.3:c.1131A>C
|
ENSP00000443246.1:p.Ser377=
|
|
ENST00000542943.5:c.942A>C
|
ENSP00000440345.1:p.Ser314=
|
|
ENST00000595085.5:c.922+334A>C
|
ENSP00000471150.2:n.922+334A>C
|
|
NM_000709.3:c.1029A>C
|
NP_000700.1:p.Ser343=
|
|
NM_001164783.1:c.1026A>C
|
NP_001158255.1:p.Ser342=
|
|
NM_000709.4:c.1029A>C
MANE Select
|
NP_000700.1:p.Ser343=
|
|
NM_001164783.2:c.1026A>C
|
NP_001158255.1:p.Ser342=
|
|