|
NM_006767.4:c.981C>G
MANE Select
|
NP_006758.2:p.Ser327Arg
|
|
ENST00000646124.2:c.981C>G
MANE Select
|
ENSP00000496779.1:p.Ser327Arg
|
|
NM_006767.3:c.981C>G
|
NP_006758.2:p.Ser327Arg
|
|
ENST00000215739.12:c.981C>G
|
ENSP00000215739.8:p.Ser327Arg
|
|
ENST00000461510.1:n.82C>G
|
|
|
ENST00000479606.5:n.1127C>G
|
|
|
ENST00000492480.1:n.37C>G
|
|
|
ENST00000495142.6:n.326C>G
|
|
|
ENST00000497716.5:n.808C>G
|
|
|
ENST00000642151.1:c.812C>G
|
|
|
ENST00000643578.1:n.1003C>G
|
|
|
ENST00000646506.1:n.560C>G
|
|
|
ENST00000700578.1:c.981C>G
|
ENSP00000515073.1:p.Ser327Arg
|