ENST00000625662.3:c.2175A>C
|
|
|
ENST00000628118.2:c.1702A>C
|
|
|
ENST00000700551.1:c.*1499A>C
|
ENSP00000515057.1:n.*1499A>C
|
|
ENST00000394196.9:c.2668A>C
MANE Select
|
ENSP00000377747.4:p.Asn890His
|
|
ENST00000635856.1:n.3240A>C
|
|
|
ENST00000636306.1:n.228A>C
|
|
|
ENST00000636881.1:c.2039A>C
|
|
|
ENST00000637572.1:n.3412A>C
|
|
|
ENST00000394196.8:c.2668A>C
|
ENSP00000377747.4:p.Asn890His
|
|
ENST00000625463.1:c.208A>C
|
ENSP00000486391.1:p.Asn70His
|
|
ENST00000626874.2:c.2668A>C
|
ENSP00000486629.1:p.Asn890His
|
|
ENST00000628118.1:n.447A>C
|
|
|
NM_001271.3:c.2668A>C
|
NP_001262.3:p.Asn890His
|
|
NM_001271.4:c.2668A>C
MANE Select
|
NP_001262.3:p.Asn890His
|
|