ENST00000673913.2:c.1664A>G
|
ENSP00000501161.2:p.Gln555Arg
|
|
ENST00000710286.1:c.2021A>G
|
ENSP00000518176.1:p.Gln674Arg
|
|
ENST00000673903.1:c.1289A>G
|
ENSP00000501257.1:p.Gln430Arg
|
|
ENST00000673913.1:c.404A>G
|
ENSP00000501161.1:p.Gln135Arg
|
|
ENST00000302118.5:c.1664A>G
MANE Select
|
ENSP00000303208.5:p.Gln555Arg
|
|
ENST00000490692.1:n.2227+999A>G
|
|
|
NM_174936.3:c.1664A>G , LRG_275t1:c.1664A>G
|
NP_777596.2:p.Gln555Arg
|
|
NR_110451.1:n.1271A>G
|
|
|
XM_011541193.1:c.785A>G
|
XP_011539495.1:p.Gln262Arg
|
|
NM_174936.4:c.1664A>G
MANE Select
|
NP_777596.2:p.Gln555Arg
|
|
NR_110451.2:n.1271A>G
|
|
|