ENST00000269980.7:c.660G=
MANE Select
|
ENSP00000269980.2:p.Ala220=
|
|
ENST00000269980.6:c.660G=
|
ENSP00000269980.2:p.Ala220=
|
|
ENST00000457836.6:c.594G=
|
ENSP00000416000.2:p.Ala198=
|
|
ENST00000535632.5:n.289G=
|
|
|
ENST00000538423.5:n.786G=
|
|
|
ENST00000540732.3:c.762G=
|
ENSP00000443246.1:p.Ala254=
|
|
ENST00000541315.1:c.560G=
|
|
|
ENST00000542943.5:c.573G=
|
ENSP00000440345.1:p.Ala191=
|
|
ENST00000545787.1:n.288G=
|
|
|
ENST00000595085.5:c.660G=
|
ENSP00000471150.2:p.Ala220=
|
|
NM_000709.3:c.660G=
|
NP_000700.1:p.Ala220=
|
|
NM_001164783.1:c.660G=
|
NP_001158255.1:p.Ala220=
|
|
NM_000709.4:c.660G=
MANE Select
|
NP_000700.1:p.Ala220=
|
|
NM_001164783.2:c.660G=
|
NP_001158255.1:p.Ala220=
|
|