ENST00000545712.7:c.696G>A
MANE Select
|
ENSP00000445920.1:p.Gly232=
|
|
ENST00000537496.5:c.*261G>A
|
ENSP00000444793.1:n.*261G>A
|
|
ENST00000540016.5:c.540G>A
|
ENSP00000474582.1:p.Gly180=
|
|
ENST00000541763.6:c.921G>A
|
ENSP00000474981.1:n.921G>A
|
|
ENST00000544051.5:c.*577G>A
|
ENSP00000438079.1:n.*577G>A
|
|
ENST00000545712.6:c.696G>A
|
ENSP00000445920.1:p.Gly232=
|
|
NM_052845.3:c.696G>A
|
NP_443077.1:p.Gly232=
|
|
NR_038118.1:n.856G>A
|
|
|
XM_011538266.1:c.*43G>A
|
XP_011536568.1:n.*43G>A
|
|
XM_011538267.1:c.*43G>A
|
XP_011536569.1:n.*43G>A
|
|
XM_011538268.1:c.423G>A
|
XP_011536570.1:p.Gly141=
|
|
XM_011538269.1:c.420G>A
|
XP_011536571.1:p.Gly140=
|
|
XM_011538267.3:c.*43G>A
|
XP_011536569.1:n.*43G>A
|
|
XM_011538268.2:c.423G>A
|
XP_011536570.1:p.Gly141=
|
|
XM_011538269.2:c.420G>A
|
XP_011536571.1:p.Gly140=
|
|
NM_052845.4:c.696G>A
MANE Select
|
NP_443077.1:p.Gly232=
|
|
NR_038118.2:n.807G>A
|
|
|