ENST00000545712.7:c.742G>C
MANE Select
|
ENSP00000445920.1:p.Glu248Gln
|
|
ENST00000537496.5:c.*307G>C
|
ENSP00000444793.1:n.*307G>C
|
|
ENST00000540016.5:c.586G>C
|
ENSP00000474582.1:p.Glu196Gln
|
|
ENST00000541763.6:c.967G>C
|
ENSP00000474981.1:n.967G>C
|
|
ENST00000544051.5:c.*623G>C
|
ENSP00000438079.1:n.*623G>C
|
|
ENST00000545712.6:c.742G>C
|
ENSP00000445920.1:p.Glu248Gln
|
|
NM_052845.3:c.742G>C
|
NP_443077.1:p.Glu248Gln
|
|
NR_038118.1:n.902G>C
|
|
|
XM_011538266.1:c.*89G>C
|
XP_011536568.1:n.*89G>C
|
|
XM_011538267.1:c.*89G>C
|
XP_011536569.1:n.*89G>C
|
|
XM_011538268.1:c.469G>C
|
XP_011536570.1:p.Glu157Gln
|
|
XM_011538269.1:c.466G>C
|
XP_011536571.1:p.Glu156Gln
|
|
XM_011538267.3:c.*89G>C
|
XP_011536569.1:n.*89G>C
|
|
XM_011538268.2:c.469G>C
|
XP_011536570.1:p.Glu157Gln
|
|
XM_011538269.2:c.466G>C
|
XP_011536571.1:p.Glu156Gln
|
|
NM_052845.4:c.742G>C
MANE Select
|
NP_443077.1:p.Glu248Gln
|
|
NR_038118.2:n.853G>C
|
|
|