ENST00000673913.2:c.1641G>A
|
ENSP00000501161.2:p.Gly547=
|
|
ENST00000710286.1:c.1998G>A
|
ENSP00000518176.1:p.Gly666=
|
|
ENST00000673903.1:c.1266G>A
|
ENSP00000501257.1:p.Gly422=
|
|
ENST00000673913.1:c.381G>A
|
ENSP00000501161.1:p.Gly127=
|
|
ENST00000302118.5:c.1641G>A
MANE Select
|
ENSP00000303208.5:p.Gly547=
|
|
ENST00000490692.1:n.2227+976G>A
|
|
|
NM_174936.3:c.1641G>A , LRG_275t1:c.1641G>A
|
NP_777596.2:p.Gly547=
|
|
NR_110451.1:n.1248G>A
|
|
|
XM_011541193.1:c.762G>A
|
XP_011539495.1:p.Gly254=
|
|
NM_174936.4:c.1641G>A
MANE Select
|
NP_777596.2:p.Gly547=
|
|
NR_110451.2:n.1248G>A
|
|
|