ENST00000673913.2:c.*207A=
|
ENSP00000501161.2:n.*207A=
|
|
ENST00000710286.1:c.2224A=
|
ENSP00000518176.1:p.Thr742=
|
|
ENST00000673903.1:c.1492A=
|
ENSP00000501257.1:p.Thr498=
|
|
ENST00000673913.1:c.717A=
|
ENSP00000501161.1:n.717A=
|
|
ENST00000302118.5:c.1867A=
MANE Select
|
ENSP00000303208.5:p.Thr623=
|
|
ENST00000490692.1:n.2413A=
|
|
|
NM_174936.3:c.1867A= , LRG_275t1:c.1867A=
|
NP_777596.2:p.Thr623=
|
|
NR_110451.1:n.1474A=
|
|
|
XM_011541193.1:c.988A=
|
XP_011539495.1:p.Thr330=
|
|
NM_174936.4:c.1867A=
MANE Select
|
NP_777596.2:p.Thr623=
|
|
NR_110451.2:n.1474A=
|
|
|