ENST00000625662.3:c.2116G>A
|
|
|
ENST00000628118.2:c.1643G>A
|
|
|
ENST00000700551.1:c.*1440G>A
|
ENSP00000515057.1:n.*1440G>A
|
|
ENST00000394196.9:c.2609G>A
MANE Select
|
ENSP00000377747.4:p.Gly870Asp
|
|
ENST00000635856.1:n.3181G>A
|
|
|
ENST00000636306.1:n.169G>A
|
|
|
ENST00000636881.1:c.1980G>A
|
|
|
ENST00000637572.1:n.3353G>A
|
|
|
ENST00000394196.8:c.2609G>A
|
ENSP00000377747.4:p.Gly870Asp
|
|
ENST00000625463.1:c.149G>A
|
ENSP00000486391.1:p.Gly50Asp
|
|
ENST00000626874.2:c.2609G>A
|
ENSP00000486629.1:p.Gly870Asp
|
|
ENST00000628118.1:n.388G>A
|
|
|
NM_001271.3:c.2609G>A
|
NP_001262.3:p.Gly870Asp
|
|
NM_001271.4:c.2609G>A
MANE Select
|
NP_001262.3:p.Gly870Asp
|
|