ENST00000673913.2:c.1668C>T
|
ENSP00000501161.2:p.Gly556=
|
|
ENST00000710286.1:c.2025C>T
|
ENSP00000518176.1:p.Gly675=
|
|
ENST00000673903.1:c.1293C>T
|
ENSP00000501257.1:p.Gly431=
|
|
ENST00000673913.1:c.408C>T
|
ENSP00000501161.1:p.Gly136=
|
|
ENST00000302118.5:c.1668C>T
MANE Select
|
ENSP00000303208.5:p.Gly556=
|
|
ENST00000490692.1:n.2227+1003C>T
|
|
|
NM_174936.3:c.1668C>T , LRG_275t1:c.1668C>T
|
NP_777596.2:p.Gly556=
|
|
NR_110451.1:n.1275C>T
|
|
|
XM_011541193.1:c.789C>T
|
XP_011539495.1:p.Gly263=
|
|
NM_174936.4:c.1668C>T
MANE Select
|
NP_777596.2:p.Gly556=
|
|
NR_110451.2:n.1275C>T
|
|
|