ENST00000673913.2:c.1614A>C
|
ENSP00000501161.2:p.Thr538=
|
|
ENST00000710286.1:c.1971A>C
|
ENSP00000518176.1:p.Thr657=
|
|
ENST00000673903.1:c.1239A>C
|
ENSP00000501257.1:p.Thr413=
|
|
ENST00000673913.1:c.354A>C
|
ENSP00000501161.1:p.Thr118=
|
|
ENST00000302118.5:c.1614A>C
MANE Select
|
ENSP00000303208.5:p.Thr538=
|
|
ENST00000490692.1:n.2227+949A>C
|
|
|
NM_174936.3:c.1614A>C , LRG_275t1:c.1614A>C
|
NP_777596.2:p.Thr538=
|
|
NR_110451.1:n.1221A>C
|
|
|
XM_011541193.1:c.735A>C
|
XP_011539495.1:p.Thr245=
|
|
NM_174936.4:c.1614A>C
MANE Select
|
NP_777596.2:p.Thr538=
|
|
NR_110451.2:n.1221A>C
|
|
|