ENST00000673913.2:c.*360G>T
|
ENSP00000501161.2:n.*360G>T
|
|
ENST00000710286.1:c.2377G>T
|
ENSP00000518176.1:p.Ala793Ser
|
|
ENST00000673903.1:c.1645G>T
|
ENSP00000501257.1:p.Ala549Ser
|
|
ENST00000673913.1:c.870G>T
|
ENSP00000501161.1:n.870G>T
|
|
ENST00000302118.5:c.2020G>T
MANE Select
|
ENSP00000303208.5:p.Ala674Ser
|
|
ENST00000490692.1:n.2566G>T
|
|
|
NM_174936.3:c.2020G>T , LRG_275t1:c.2020G>T
|
NP_777596.2:p.Ala674Ser
|
|
NR_110451.1:n.1627G>T
|
|
|
XM_011541193.1:c.1141G>T
|
XP_011539495.1:p.Ala381Ser
|
|
NM_174936.4:c.2020G>T
MANE Select
|
NP_777596.2:p.Ala674Ser
|
|
NR_110451.2:n.1627G>T
|
|
|