ENST00000545712.7:c.712T>G
MANE Select
|
ENSP00000445920.1:p.Tyr238Asp
|
|
ENST00000537496.5:c.*277T>G
|
ENSP00000444793.1:n.*277T>G
|
|
ENST00000540016.5:c.556T>G
|
ENSP00000474582.1:p.Tyr186Asp
|
|
ENST00000541763.6:c.937T>G
|
ENSP00000474981.1:n.937T>G
|
|
ENST00000544051.5:c.*593T>G
|
ENSP00000438079.1:n.*593T>G
|
|
ENST00000545712.6:c.712T>G
|
ENSP00000445920.1:p.Tyr238Asp
|
|
NM_052845.3:c.712T>G
|
NP_443077.1:p.Tyr238Asp
|
|
NR_038118.1:n.872T>G
|
|
|
XM_011538266.1:c.*59T>G
|
XP_011536568.1:n.*59T>G
|
|
XM_011538267.1:c.*59T>G
|
XP_011536569.1:n.*59T>G
|
|
XM_011538268.1:c.439T>G
|
XP_011536570.1:p.Tyr147Asp
|
|
XM_011538269.1:c.436T>G
|
XP_011536571.1:p.Tyr146Asp
|
|
XM_011538267.3:c.*59T>G
|
XP_011536569.1:n.*59T>G
|
|
XM_011538268.2:c.439T>G
|
XP_011536570.1:p.Tyr147Asp
|
|
XM_011538269.2:c.436T>G
|
XP_011536571.1:p.Tyr146Asp
|
|
NM_052845.4:c.712T>G
MANE Select
|
NP_443077.1:p.Tyr238Asp
|
|
NR_038118.2:n.823T>G
|
|
|