ENST00000673913.2:c.1552G>C
|
ENSP00000501161.2:p.Glu518Gln
|
|
ENST00000710286.1:c.1909G>C
|
ENSP00000518176.1:p.Glu637Gln
|
|
ENST00000673903.1:c.1177G>C
|
ENSP00000501257.1:p.Glu393Gln
|
|
ENST00000673913.1:c.292G>C
|
ENSP00000501161.1:p.Glu98Gln
|
|
ENST00000302118.5:c.1552G>C
MANE Select
|
ENSP00000303208.5:p.Glu518Gln
|
|
ENST00000490692.1:n.2227+887G>C
|
|
|
NM_174936.3:c.1552G>C , LRG_275t1:c.1552G>C
|
NP_777596.2:p.Glu518Gln
|
|
NR_110451.1:n.1159G>C
|
|
|
XM_011541193.1:c.673G>C
|
XP_011539495.1:p.Glu225Gln
|
|
NM_174936.4:c.1552G>C
MANE Select
|
NP_777596.2:p.Glu518Gln
|
|
NR_110451.2:n.1159G>C
|
|
|