|
NM_006767.4:c.1901A>C
MANE Select
|
NP_006758.2:p.Gln634Pro
|
|
ENST00000646124.2:c.1901A>C
MANE Select
|
ENSP00000496779.1:p.Gln634Pro
|
|
NM_006767.3:c.1901A>C
|
NP_006758.2:p.Gln634Pro
|
|
ENST00000215739.12:c.1901A>C
|
ENSP00000215739.8:p.Gln634Pro
|
|
ENST00000415354.6:c.213A>C
|
ENSP00000393765.2:p.Ala71=
|
|
ENST00000415817.2:c.213A>C
|
|
|
ENST00000439171.5:c.183A>C
|
|
|
ENST00000452988.5:c.80A>C
|
ENSP00000408789.1:p.Gln27Pro
|
|
ENST00000464807.1:n.162A>C
|
|
|
ENST00000479606.5:n.2047A>C
|
|
|
ENST00000491432.5:n.322A>C
|
|
|
ENST00000495142.5:n.517A>C
|
|
|
ENST00000495142.6:n.1534A>C
|
|
|
ENST00000642151.1:c.1732A>C
|
|
|
ENST00000643578.1:n.1923A>C
|
|
|
ENST00000643710.1:n.762A>C
|
|
|
ENST00000646506.1:n.1768A>C
|
|
|
ENST00000700578.1:c.1901A>C
|
ENSP00000515073.1:p.Gln634Pro
|