ENST00000673913.2:c.1587A>G
|
ENSP00000501161.2:p.Leu529=
|
|
ENST00000710286.1:c.1944A>G
|
ENSP00000518176.1:p.Leu648=
|
|
ENST00000673903.1:c.1212A>G
|
ENSP00000501257.1:p.Leu404=
|
|
ENST00000673913.1:c.327A>G
|
ENSP00000501161.1:p.Leu109=
|
|
ENST00000302118.5:c.1587A>G
MANE Select
|
ENSP00000303208.5:p.Leu529=
|
|
ENST00000490692.1:n.2227+922A>G
|
|
|
NM_174936.3:c.1587A>G , LRG_275t1:c.1587A>G
|
NP_777596.2:p.Leu529=
|
|
NR_110451.1:n.1194A>G
|
|
|
XM_011541193.1:c.708A>G
|
XP_011539495.1:p.Leu236=
|
|
NM_174936.4:c.1587A>G
MANE Select
|
NP_777596.2:p.Leu529=
|
|
NR_110451.2:n.1194A>G
|
|
|