|
NM_006767.4:c.2076T>A
MANE Select
|
NP_006758.2:p.Phe692Leu
|
|
ENST00000646124.2:c.2076T>A
MANE Select
|
ENSP00000496779.1:p.Phe692Leu
|
|
NM_006767.3:c.2076T>A
|
NP_006758.2:p.Phe692Leu
|
|
ENST00000215739.12:c.2076T>A
|
ENSP00000215739.8:p.Phe692Leu
|
|
ENST00000415354.6:c.505T>A
|
ENSP00000393765.2:n.505T>A
|
|
ENST00000415817.2:c.505T>A
|
|
|
ENST00000439171.5:c.475T>A
|
|
|
ENST00000452988.5:c.238T>A
|
ENSP00000408789.1:n.238T>A
|
|
ENST00000463909.1:n.791T>A
|
|
|
ENST00000479606.5:n.2222T>A
|
|
|
ENST00000491432.5:n.497T>A
|
|
|
ENST00000495142.5:n.692T>A
|
|
|
ENST00000495142.6:n.2428T>A
|
|
|
ENST00000498649.1:n.92T>A
|
|
|
ENST00000642151.1:c.1907T>A
|
|
|
ENST00000643578.1:n.2098T>A
|
|
|
ENST00000643710.1:n.937T>A
|
|
|
ENST00000646506.1:n.1943T>A
|
|
|
ENST00000700578.1:c.2076T>A
|
ENSP00000515073.1:p.Phe692Leu
|