ENST00000625662.3:c.2201A>C
|
|
|
ENST00000628118.2:c.1728A>C
|
|
|
ENST00000700551.1:c.*1525A>C
|
ENSP00000515057.1:n.*1525A>C
|
|
ENST00000394196.9:c.2694A>C
MANE Select
|
ENSP00000377747.4:p.Gln898His
|
|
ENST00000635856.1:n.3266A>C
|
|
|
ENST00000636306.1:n.254A>C
|
|
|
ENST00000636881.1:c.2065A>C
|
|
|
ENST00000637572.1:n.3438A>C
|
|
|
ENST00000394196.8:c.2694A>C
|
ENSP00000377747.4:p.Gln898His
|
|
ENST00000625463.1:c.234A>C
|
ENSP00000486391.1:p.Gln78His
|
|
ENST00000626874.2:c.2694A>C
|
ENSP00000486629.1:p.Gln898His
|
|
ENST00000628118.1:n.473A>C
|
|
|
NM_001271.3:c.2694A>C
|
NP_001262.3:p.Gln898His
|
|
NM_001271.4:c.2694A>C
MANE Select
|
NP_001262.3:p.Gln898His
|
|