ENST00000673913.2:c.*178A>G
|
ENSP00000501161.2:n.*178A>G
|
|
ENST00000710286.1:c.2195A>G
|
ENSP00000518176.1:p.His732Arg
|
|
ENST00000673903.1:c.1463A>G
|
ENSP00000501257.1:p.His488Arg
|
|
ENST00000673913.1:c.688A>G
|
ENSP00000501161.1:n.688A>G
|
|
ENST00000302118.5:c.1838A>G
MANE Select
|
ENSP00000303208.5:p.His613Arg
|
|
ENST00000490692.1:n.2384A>G
|
|
|
NM_174936.3:c.1838A>G , LRG_275t1:c.1838A>G
|
NP_777596.2:p.His613Arg
|
|
NR_110451.1:n.1445A>G
|
|
|
XM_011541193.1:c.959A>G
|
XP_011539495.1:p.His320Arg
|
|
NM_174936.4:c.1838A>G
MANE Select
|
NP_777596.2:p.His613Arg
|
|
NR_110451.2:n.1445A>G
|
|
|