ENST00000545712.7:c.743A>G
MANE Select
|
ENSP00000445920.1:p.Glu248Gly
|
|
ENST00000537496.5:c.*308A>G
|
ENSP00000444793.1:n.*308A>G
|
|
ENST00000540016.5:c.587A>G
|
ENSP00000474582.1:p.Glu196Gly
|
|
ENST00000541763.6:c.968A>G
|
ENSP00000474981.1:n.968A>G
|
|
ENST00000544051.5:c.*624A>G
|
ENSP00000438079.1:n.*624A>G
|
|
ENST00000545712.6:c.743A>G
|
ENSP00000445920.1:p.Glu248Gly
|
|
NM_052845.3:c.743A>G
|
NP_443077.1:p.Glu248Gly
|
|
NR_038118.1:n.903A>G
|
|
|
XM_011538266.1:c.*90A>G
|
XP_011536568.1:n.*90A>G
|
|
XM_011538267.1:c.*90A>G
|
XP_011536569.1:n.*90A>G
|
|
XM_011538268.1:c.470A>G
|
XP_011536570.1:p.Glu157Gly
|
|
XM_011538269.1:c.467A>G
|
XP_011536571.1:p.Glu156Gly
|
|
XM_011538267.3:c.*90A>G
|
XP_011536569.1:n.*90A>G
|
|
XM_011538268.2:c.470A>G
|
XP_011536570.1:p.Glu157Gly
|
|
XM_011538269.2:c.467A>G
|
XP_011536571.1:p.Glu156Gly
|
|
NM_052845.4:c.743A>G
MANE Select
|
NP_443077.1:p.Glu248Gly
|
|
NR_038118.2:n.854A>G
|
|
|