ENST00000673913.2:c.1591C>G
|
ENSP00000501161.2:p.Gln531Glu
|
|
ENST00000710286.1:c.1948C>G
|
ENSP00000518176.1:p.Gln650Glu
|
|
ENST00000673903.1:c.1216C>G
|
ENSP00000501257.1:p.Gln406Glu
|
|
ENST00000673913.1:c.331C>G
|
ENSP00000501161.1:p.Gln111Glu
|
|
ENST00000302118.5:c.1591C>G
MANE Select
|
ENSP00000303208.5:p.Gln531Glu
|
|
ENST00000490692.1:n.2227+926C>G
|
|
|
NM_174936.3:c.1591C>G , LRG_275t1:c.1591C>G
|
NP_777596.2:p.Gln531Glu
|
|
NR_110451.1:n.1198C>G
|
|
|
XM_011541193.1:c.712C>G
|
XP_011539495.1:p.Gln238Glu
|
|
NM_174936.4:c.1591C>G
MANE Select
|
NP_777596.2:p.Gln531Glu
|
|
NR_110451.2:n.1198C>G
|
|
|