|
NM_006767.4:c.2002G>T
MANE Select
|
NP_006758.2:p.Asp668Tyr
|
|
ENST00000646124.2:c.2002G>T
MANE Select
|
ENSP00000496779.1:p.Asp668Tyr
|
|
NM_006767.3:c.2002G>T
|
NP_006758.2:p.Asp668Tyr
|
|
ENST00000215739.12:c.2002G>T
|
ENSP00000215739.8:p.Asp668Tyr
|
|
ENST00000415354.6:c.431G>T
|
ENSP00000393765.2:n.431G>T
|
|
ENST00000415817.2:c.431G>T
|
|
|
ENST00000439171.5:c.401G>T
|
|
|
ENST00000452988.5:c.164G>T
|
ENSP00000408789.1:p.Ter55Leu
|
|
ENST00000463909.1:n.717G>T
|
|
|
ENST00000479606.5:n.2148G>T
|
|
|
ENST00000491432.5:n.423G>T
|
|
|
ENST00000495142.5:n.618G>T
|
|
|
ENST00000495142.6:n.2354G>T
|
|
|
ENST00000498649.1:n.18G>T
|
|
|
ENST00000642151.1:c.1833G>T
|
|
|
ENST00000643578.1:n.2024G>T
|
|
|
ENST00000643710.1:n.863G>T
|
|
|
ENST00000646506.1:n.1869G>T
|
|
|
ENST00000700578.1:c.2002G>T
|
ENSP00000515073.1:p.Asp668Tyr
|