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NM_006767.4:c.1856G>A
MANE Select
|
NP_006758.2:p.Arg619His
|
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ENST00000646124.2:c.1856G>A
MANE Select
|
ENSP00000496779.1:p.Arg619His
|
|
NM_006767.3:c.1856G>A
|
NP_006758.2:p.Arg619His
|
|
ENST00000215739.12:c.1856G>A
|
ENSP00000215739.8:p.Arg619His
|
|
ENST00000415354.6:c.168G>A
|
ENSP00000393765.2:p.Ala56=
|
|
ENST00000415817.2:c.168G>A
|
|
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ENST00000439171.5:c.138G>A
|
|
|
ENST00000452988.5:c.35G>A
|
ENSP00000408789.1:p.Arg12His
|
|
ENST00000464807.1:n.117G>A
|
|
|
ENST00000479606.5:n.2002G>A
|
|
|
ENST00000491432.5:n.277G>A
|
|
|
ENST00000495142.5:n.472G>A
|
|
|
ENST00000495142.6:n.1489G>A
|
|
|
ENST00000642151.1:c.1687G>A
|
|
|
ENST00000643578.1:n.1878G>A
|
|
|
ENST00000643710.1:n.717G>A
|
|
|
ENST00000646506.1:n.1723G>A
|
|
|
ENST00000700578.1:c.1856G>A
|
ENSP00000515073.1:p.Arg619His
|