|
NM_006767.4:c.2406G>A
MANE Select
|
NP_006758.2:p.Lys802=
|
|
ENST00000646124.2:c.2406G>A
MANE Select
|
ENSP00000496779.1:p.Lys802=
|
|
NM_006767.3:c.2406G>A
|
NP_006758.2:p.Lys802=
|
|
ENST00000215739.12:c.2406G>A
|
ENSP00000215739.8:p.Lys802=
|
|
ENST00000415817.1:c.304G>A
|
|
|
ENST00000415817.2:c.835G>A
|
|
|
ENST00000452988.5:c.568G>A
|
ENSP00000408789.1:n.568G>A
|
|
ENST00000463909.1:n.1704G>A
|
|
|
ENST00000479606.5:n.2552G>A
|
|
|
ENST00000495142.6:n.2758G>A
|
|
|
ENST00000498649.1:n.506G>A
|
|
|
ENST00000642151.1:c.2237G>A
|
|
|
ENST00000643578.1:n.2428G>A
|
|
|
ENST00000643710.1:n.1267G>A
|
|
|
ENST00000646506.1:n.2273G>A
|
|
|
ENST00000700578.1:c.2325+165G>A
|
ENSP00000515073.1:n.2325+165G>A
|