ENST00000269980.7:c.1006C>A
MANE Select
|
ENSP00000269980.2:p.His336Asn
|
|
ENST00000269980.6:c.1006C>A
|
ENSP00000269980.2:p.His336Asn
|
|
ENST00000457836.6:c.1015C>A
|
ENSP00000416000.2:p.His339Asn
|
|
ENST00000540732.3:c.1108C>A
|
ENSP00000443246.1:p.His370Asn
|
|
ENST00000542943.5:c.919C>A
|
ENSP00000440345.1:p.His307Asn
|
|
ENST00000595085.5:c.922+311C>A
|
ENSP00000471150.2:n.922+311C>A
|
|
NM_000709.3:c.1006C>A
|
NP_000700.1:p.His336Asn
|
|
NM_001164783.1:c.1003C>A
|
NP_001158255.1:p.His335Asn
|
|
NM_000709.4:c.1006C>A
MANE Select
|
NP_000700.1:p.His336Asn
|
|
NM_001164783.2:c.1003C>A
|
NP_001158255.1:p.His335Asn
|
|