ENST00000673913.2:c.*343G=
|
ENSP00000501161.2:n.*343G=
|
|
ENST00000710286.1:c.2360G=
|
ENSP00000518176.1:p.Ser787=
|
|
ENST00000673903.1:c.1628G=
|
ENSP00000501257.1:p.Ser543=
|
|
ENST00000673913.1:c.853G=
|
ENSP00000501161.1:n.853G=
|
|
ENST00000302118.5:c.2003G=
MANE Select
|
ENSP00000303208.5:p.Ser668=
|
|
ENST00000490692.1:n.2549G=
|
|
|
NM_174936.3:c.2003G= , LRG_275t1:c.2003G=
|
NP_777596.2:p.Ser668=
|
|
NR_110451.1:n.1610G=
|
|
|
XM_011541193.1:c.1124G=
|
XP_011539495.1:p.Ser375=
|
|
NM_174936.4:c.2003G=
MANE Select
|
NP_777596.2:p.Ser668=
|
|
NR_110451.2:n.1610G=
|
|
|