ENST00000682012.1:n.561T>G
|
|
|
ENST00000684569.1:n.531T>G
|
|
|
ENST00000561421.6:c.486T>G
MANE Select
|
ENSP00000453347.2:p.Arg162=
|
|
ENST00000646551.1:n.2113T>G
|
|
|
ENST00000261755.9:c.486T>G
|
ENSP00000261755.5:p.Arg162=
|
|
ENST00000407106.5:c.486T>G
|
ENSP00000385080.1:p.Arg162=
|
|
ENST00000539156.5:c.276T>G
|
ENSP00000454271.1:p.Arg92=
|
|
ENST00000558514.1:n.32T>G
|
|
|
ENST00000558627.1:n.414T>G
|
|
|
ENST00000561421.5:c.486T>G
|
ENSP00000453347.1:p.Arg162=
|
|
NM_000137.2:c.486T>G
|
NP_000128.1:p.Arg162=
|
|
XM_024449872.1:c.486T>G
|
XP_024305640.1:p.Arg162=
|
|
NM_000137.4:c.486T>G
MANE Select
|
NP_000128.1:p.Arg162=
|
|
NM_001374377.1:c.486T>G
|
NP_001361306.1:p.Arg162=
|
|
NM_001374380.1:c.486T>G
|
NP_001361309.1:p.Arg162=
|
|