ENST00000545712.7:c.713A>T
MANE Select
|
ENSP00000445920.1:p.Tyr238Phe
|
|
ENST00000537496.5:c.*278A>T
|
ENSP00000444793.1:n.*278A>T
|
|
ENST00000540016.5:c.557A>T
|
ENSP00000474582.1:p.Tyr186Phe
|
|
ENST00000541763.6:c.938A>T
|
ENSP00000474981.1:n.938A>T
|
|
ENST00000544051.5:c.*594A>T
|
ENSP00000438079.1:n.*594A>T
|
|
ENST00000545712.6:c.713A>T
|
ENSP00000445920.1:p.Tyr238Phe
|
|
NM_052845.3:c.713A>T
|
NP_443077.1:p.Tyr238Phe
|
|
NR_038118.1:n.873A>T
|
|
|
XM_011538266.1:c.*60A>T
|
XP_011536568.1:n.*60A>T
|
|
XM_011538267.1:c.*60A>T
|
XP_011536569.1:n.*60A>T
|
|
XM_011538268.1:c.440A>T
|
XP_011536570.1:p.Tyr147Phe
|
|
XM_011538269.1:c.437A>T
|
XP_011536571.1:p.Tyr146Phe
|
|
XM_011538267.3:c.*60A>T
|
XP_011536569.1:n.*60A>T
|
|
XM_011538268.2:c.440A>T
|
XP_011536570.1:p.Tyr147Phe
|
|
XM_011538269.2:c.437A>T
|
XP_011536571.1:p.Tyr146Phe
|
|
NM_052845.4:c.713A>T
MANE Select
|
NP_443077.1:p.Tyr238Phe
|
|
NR_038118.2:n.824A>T
|
|
|