|
NM_006767.4:c.1939A>G
MANE Select
|
NP_006758.2:p.Ile647Val
|
|
ENST00000646124.2:c.1939A>G
MANE Select
|
ENSP00000496779.1:p.Ile647Val
|
|
NM_006767.3:c.1939A>G
|
NP_006758.2:p.Ile647Val
|
|
ENST00000215739.12:c.1939A>G
|
ENSP00000215739.8:p.Ile647Val
|
|
ENST00000415354.6:c.251A>G
|
ENSP00000393765.2:p.His84Arg
|
|
ENST00000415817.2:c.251A>G
|
|
|
ENST00000439171.5:c.221A>G
|
|
|
ENST00000452988.5:c.118A>G
|
ENSP00000408789.1:p.Ile40Val
|
|
ENST00000464807.1:n.200A>G
|
|
|
ENST00000479606.5:n.2085A>G
|
|
|
ENST00000491432.5:n.360A>G
|
|
|
ENST00000495142.5:n.555A>G
|
|
|
ENST00000495142.6:n.1572A>G
|
|
|
ENST00000642151.1:c.1770A>G
|
|
|
ENST00000643578.1:n.1961A>G
|
|
|
ENST00000643710.1:n.800A>G
|
|
|
ENST00000646506.1:n.1806A>G
|
|
|
ENST00000700578.1:c.1939A>G
|
ENSP00000515073.1:p.Ile647Val
|