ENST00000545712.7:c.720A>G
MANE Select
|
ENSP00000445920.1:p.Lys240=
|
|
ENST00000537496.5:c.*285A>G
|
ENSP00000444793.1:n.*285A>G
|
|
ENST00000540016.5:c.564A>G
|
ENSP00000474582.1:p.Lys188=
|
|
ENST00000541763.6:c.945A>G
|
ENSP00000474981.1:n.945A>G
|
|
ENST00000544051.5:c.*601A>G
|
ENSP00000438079.1:n.*601A>G
|
|
ENST00000545712.6:c.720A>G
|
ENSP00000445920.1:p.Lys240=
|
|
NM_052845.3:c.720A>G
|
NP_443077.1:p.Lys240=
|
|
NR_038118.1:n.880A>G
|
|
|
XM_011538266.1:c.*67A>G
|
XP_011536568.1:n.*67A>G
|
|
XM_011538267.1:c.*67A>G
|
XP_011536569.1:n.*67A>G
|
|
XM_011538268.1:c.447A>G
|
XP_011536570.1:p.Lys149=
|
|
XM_011538269.1:c.444A>G
|
XP_011536571.1:p.Lys148=
|
|
XM_011538267.3:c.*67A>G
|
XP_011536569.1:n.*67A>G
|
|
XM_011538268.2:c.447A>G
|
XP_011536570.1:p.Lys149=
|
|
XM_011538269.2:c.444A>G
|
XP_011536571.1:p.Lys148=
|
|
NM_052845.4:c.720A>G
MANE Select
|
NP_443077.1:p.Lys240=
|
|
NR_038118.2:n.831A>G
|
|
|