ENST00000673913.2:c.1601G=
|
ENSP00000501161.2:p.Cys534=
|
|
ENST00000710286.1:c.1958G=
|
ENSP00000518176.1:p.Cys653=
|
|
ENST00000673903.1:c.1226G=
|
ENSP00000501257.1:p.Cys409=
|
|
ENST00000673913.1:c.341G=
|
ENSP00000501161.1:p.Cys114=
|
|
ENST00000302118.5:c.1601G=
MANE Select
|
ENSP00000303208.5:p.Cys534=
|
|
ENST00000490692.1:n.2227+936G=
|
|
|
NM_174936.3:c.1601G= , LRG_275t1:c.1601G=
|
NP_777596.2:p.Cys534=
|
|
NR_110451.1:n.1208G=
|
|
|
XM_011541193.1:c.722G=
|
XP_011539495.1:p.Cys241=
|
|
NM_174936.4:c.1601G=
MANE Select
|
NP_777596.2:p.Cys534=
|
|
NR_110451.2:n.1208G=
|
|
|