|
NM_006767.4:c.2074T>C
MANE Select
|
NP_006758.2:p.Phe692Leu
|
|
ENST00000646124.2:c.2074T>C
MANE Select
|
ENSP00000496779.1:p.Phe692Leu
|
|
NM_006767.3:c.2074T>C
|
NP_006758.2:p.Phe692Leu
|
|
ENST00000215739.12:c.2074T>C
|
ENSP00000215739.8:p.Phe692Leu
|
|
ENST00000415354.6:c.503T>C
|
ENSP00000393765.2:n.503T>C
|
|
ENST00000415817.2:c.503T>C
|
|
|
ENST00000439171.5:c.473T>C
|
|
|
ENST00000452988.5:c.236T>C
|
ENSP00000408789.1:n.236T>C
|
|
ENST00000463909.1:n.789T>C
|
|
|
ENST00000479606.5:n.2220T>C
|
|
|
ENST00000491432.5:n.495T>C
|
|
|
ENST00000495142.5:n.690T>C
|
|
|
ENST00000495142.6:n.2426T>C
|
|
|
ENST00000498649.1:n.90T>C
|
|
|
ENST00000642151.1:c.1905T>C
|
|
|
ENST00000643578.1:n.2096T>C
|
|
|
ENST00000643710.1:n.935T>C
|
|
|
ENST00000646506.1:n.1941T>C
|
|
|
ENST00000700578.1:c.2074T>C
|
ENSP00000515073.1:p.Phe692Leu
|