|
NM_006767.4:c.2428C>T
MANE Select
|
NP_006758.2:p.Arg810Trp
|
|
ENST00000646124.2:c.2428C>T
MANE Select
|
ENSP00000496779.1:p.Arg810Trp
|
|
NM_006767.3:c.2428C>T
|
NP_006758.2:p.Arg810Trp
|
|
ENST00000215739.12:c.2428C>T
|
ENSP00000215739.8:p.Arg810Trp
|
|
ENST00000415817.1:c.591C>T
|
|
|
ENST00000415817.2:c.857C>T
|
|
|
ENST00000452988.5:c.590C>T
|
ENSP00000408789.1:n.590C>T
|
|
ENST00000463909.1:n.1726C>T
|
|
|
ENST00000479606.5:n.2574C>T
|
|
|
ENST00000495142.6:n.2780C>T
|
|
|
ENST00000498649.1:n.528C>T
|
|
|
ENST00000642151.1:c.2259C>T
|
|
|
ENST00000643578.1:n.2450C>T
|
|
|
ENST00000643710.1:n.1289C>T
|
|
|
ENST00000646506.1:n.2295C>T
|
|
|
ENST00000700578.1:c.2347C>T
|
ENSP00000515073.1:p.Arg783Trp
|