ENST00000673913.2:c.*141T=
|
ENSP00000501161.2:n.*141T=
|
|
ENST00000710286.1:c.2158T=
|
ENSP00000518176.1:p.Cys720=
|
|
ENST00000673903.1:c.1426T=
|
ENSP00000501257.1:p.Cys476=
|
|
ENST00000673913.1:c.651T=
|
ENSP00000501161.1:n.651T=
|
|
ENST00000302118.5:c.1801T=
MANE Select
|
ENSP00000303208.5:p.Cys601=
|
|
ENST00000490692.1:n.2347T=
|
|
|
NM_174936.3:c.1801T= , LRG_275t1:c.1801T=
|
NP_777596.2:p.Cys601=
|
|
NR_110451.1:n.1408T=
|
|
|
XM_011541193.1:c.922T=
|
XP_011539495.1:p.Cys308=
|
|
NM_174936.4:c.1801T=
MANE Select
|
NP_777596.2:p.Cys601=
|
|
NR_110451.2:n.1408T=
|
|
|