ENST00000673913.2:c.*222G>C
|
ENSP00000501161.2:n.*222G>C
|
|
ENST00000710286.1:c.2239G>C
|
ENSP00000518176.1:p.Glu747Gln
|
|
ENST00000673903.1:c.1507G>C
|
ENSP00000501257.1:p.Glu503Gln
|
|
ENST00000673913.1:c.732G>C
|
ENSP00000501161.1:n.732G>C
|
|
ENST00000302118.5:c.1882G>C
MANE Select
|
ENSP00000303208.5:p.Glu628Gln
|
|
ENST00000490692.1:n.2428G>C
|
|
|
NM_174936.3:c.1882G>C , LRG_275t1:c.1882G>C
|
NP_777596.2:p.Glu628Gln
|
|
NR_110451.1:n.1489G>C
|
|
|
XM_011541193.1:c.1003G>C
|
XP_011539495.1:p.Glu335Gln
|
|
NM_174936.4:c.1882G>C
MANE Select
|
NP_777596.2:p.Glu628Gln
|
|
NR_110451.2:n.1489G>C
|
|
|