ENST00000223051.8:c.822C>A
MANE Select
|
ENSP00000223051.3:p.Arg274=
|
|
ENST00000223051.7:c.822C>A
|
ENSP00000223051.3:p.Arg274=
|
|
ENST00000431692.5:c.822C>A
|
ENSP00000413905.1:p.Arg274=
|
|
ENST00000462090.5:n.63C>A
|
|
|
ENST00000462107.1:c.822C>A
|
ENSP00000420525.1:p.Arg274=
|
|
ENST00000465294.5:n.827C>A
|
|
|
ENST00000473374.5:n.272C>A
|
|
|
ENST00000473571.1:n.276C>A
|
|
|
ENST00000475011.1:n.351C>A
|
|
|
ENST00000476304.5:n.443C>A
|
|
|
ENST00000490084.5:c.77C>A
|
|
|
NM_001206855.1:c.309C>A
|
NP_001193784.1:p.Arg103=
|
|
NM_003227.3:c.822C>A
|
NP_003218.2:p.Arg274=
|
|
XM_005250553.3:c.822C>A
|
XP_005250610.1:p.Arg274=
|
|
XM_005250554.3:c.822C>A
|
XP_005250611.1:p.Arg274=
|
|
NM_001206855.2:c.309C>A
|
NP_001193784.1:p.Arg103=
|
|
XM_005250553.4:c.822C>A
|
XP_005250610.1:p.Arg274=
|
|
XM_017012573.1:c.822C>A
|
XP_016868062.1:p.Arg274=
|
|
NM_003227.4:c.822C>A
MANE Select
|
NP_003218.2:p.Arg274=
|
|
NM_001206855.3:c.309C>A
|
NP_001193784.1:p.Arg103=
|
|