ENST00000673913.2:c.*111C>T
|
ENSP00000501161.2:n.*111C>T
|
|
ENST00000710286.1:c.2128C>T
|
ENSP00000518176.1:p.His710Tyr
|
|
ENST00000673903.1:c.1396C>T
|
ENSP00000501257.1:p.His466Tyr
|
|
ENST00000673913.1:c.621C>T
|
ENSP00000501161.1:n.621C>T
|
|
ENST00000302118.5:c.1771C>T
MANE Select
|
ENSP00000303208.5:p.His591Tyr
|
|
ENST00000490692.1:n.2317C>T
|
|
|
NM_174936.3:c.1771C>T , LRG_275t1:c.1771C>T
|
NP_777596.2:p.His591Tyr
|
|
NR_110451.1:n.1378C>T
|
|
|
XM_011541193.1:c.892C>T
|
XP_011539495.1:p.His298Tyr
|
|
NM_174936.4:c.1771C>T
MANE Select
|
NP_777596.2:p.His591Tyr
|
|
NR_110451.2:n.1378C>T
|
|
|