ENST00000545712.7:c.667C>T
MANE Select
|
ENSP00000445920.1:p.Leu223=
|
|
ENST00000537496.5:c.*232C>T
|
ENSP00000444793.1:n.*232C>T
|
|
ENST00000540016.5:c.511C>T
|
ENSP00000474582.1:p.Leu171=
|
|
ENST00000541763.6:c.892C>T
|
ENSP00000474981.1:n.892C>T
|
|
ENST00000544051.5:c.*548C>T
|
ENSP00000438079.1:n.*548C>T
|
|
ENST00000545712.6:c.667C>T
|
ENSP00000445920.1:p.Leu223=
|
|
NM_052845.3:c.667C>T
|
NP_443077.1:p.Leu223=
|
|
NR_038118.1:n.827C>T
|
|
|
XM_011538266.1:c.*14C>T
|
XP_011536568.1:n.*14C>T
|
|
XM_011538267.1:c.*14C>T
|
XP_011536569.1:n.*14C>T
|
|
XM_011538268.1:c.394C>T
|
XP_011536570.1:p.Leu132=
|
|
XM_011538269.1:c.391C>T
|
XP_011536571.1:p.Leu131=
|
|
XM_011538267.3:c.*14C>T
|
XP_011536569.1:n.*14C>T
|
|
XM_011538268.2:c.394C>T
|
XP_011536570.1:p.Leu132=
|
|
XM_011538269.2:c.391C>T
|
XP_011536571.1:p.Leu131=
|
|
NM_052845.4:c.667C>T
MANE Select
|
NP_443077.1:p.Leu223=
|
|
NR_038118.2:n.778C>T
|
|
|