ENST00000673913.2:c.1553A>G
|
ENSP00000501161.2:p.Glu518Gly
|
|
ENST00000710286.1:c.1910A>G
|
ENSP00000518176.1:p.Glu637Gly
|
|
ENST00000673903.1:c.1178A>G
|
ENSP00000501257.1:p.Glu393Gly
|
|
ENST00000673913.1:c.293A>G
|
ENSP00000501161.1:p.Glu98Gly
|
|
ENST00000302118.5:c.1553A>G
MANE Select
|
ENSP00000303208.5:p.Glu518Gly
|
|
ENST00000490692.1:n.2227+888A>G
|
|
|
NM_174936.3:c.1553A>G , LRG_275t1:c.1553A>G
|
NP_777596.2:p.Glu518Gly
|
|
NR_110451.1:n.1160A>G
|
|
|
XM_011541193.1:c.674A>G
|
XP_011539495.1:p.Glu225Gly
|
|
NM_174936.4:c.1553A>G
MANE Select
|
NP_777596.2:p.Glu518Gly
|
|
NR_110451.2:n.1160A>G
|
|
|