ENST00000673913.2:c.1631C>G
|
ENSP00000501161.2:p.Ala544Gly
|
|
ENST00000710286.1:c.1988C>G
|
ENSP00000518176.1:p.Ala663Gly
|
|
ENST00000673903.1:c.1256C>G
|
ENSP00000501257.1:p.Ala419Gly
|
|
ENST00000673913.1:c.371C>G
|
ENSP00000501161.1:p.Ala124Gly
|
|
ENST00000302118.5:c.1631C>G
MANE Select
|
ENSP00000303208.5:p.Ala544Gly
|
|
ENST00000490692.1:n.2227+966C>G
|
|
|
NM_174936.3:c.1631C>G , LRG_275t1:c.1631C>G
|
NP_777596.2:p.Ala544Gly
|
|
NR_110451.1:n.1238C>G
|
|
|
XM_011541193.1:c.752C>G
|
XP_011539495.1:p.Ala251Gly
|
|
NM_174936.4:c.1631C>G
MANE Select
|
NP_777596.2:p.Ala544Gly
|
|
NR_110451.2:n.1238C>G
|
|
|