|
NM_006767.4:c.985G>A
MANE Select
|
NP_006758.2:p.Asp329Asn
|
|
ENST00000646124.2:c.985G>A
MANE Select
|
ENSP00000496779.1:p.Asp329Asn
|
|
NM_006767.3:c.985G>A
|
NP_006758.2:p.Asp329Asn
|
|
ENST00000215739.12:c.985G>A
|
ENSP00000215739.8:p.Asp329Asn
|
|
ENST00000461510.1:n.86G>A
|
|
|
ENST00000479606.5:n.1131G>A
|
|
|
ENST00000492480.1:n.41G>A
|
|
|
ENST00000495142.6:n.330G>A
|
|
|
ENST00000497716.5:n.812G>A
|
|
|
ENST00000642151.1:c.816G>A
|
|
|
ENST00000643578.1:n.1007G>A
|
|
|
ENST00000646506.1:n.564G>A
|
|
|
ENST00000700578.1:c.985G>A
|
ENSP00000515073.1:p.Asp329Asn
|