NM_000453.3:c.1183G>A
MANE Select
|
NP_000444.1:p.Gly395Arg
|
ENST00000222248.4:c.1183G>A
MANE Select
|
ENSP00000222248.2:p.Gly395Arg
|
NM_000453.2:c.1183G>A
|
NP_000444.1:p.Gly395Arg
|
ENST00000222248.3:c.1183G>A
|
ENSP00000222248.2:p.Gly395Arg
|
ENST00000597109.1:n.182G>A
|
|
XM_011528192.1:c.1216G>A
|
XP_011526494.1:p.Gly406Arg
|
XM_011528192.2:c.1216G>A
|
XP_011526494.1:p.Gly406Arg
|
XM_011528193.1:c.949G>A
|
XP_011526495.1:p.Gly317Arg
|
XM_011528193.3:c.949G>A
|
XP_011526495.1:p.Gly317Arg
|
XM_011528194.1:c.850G>A
|
XP_011526496.1:p.Gly284Arg
|
XM_011528194.3:c.850G>A
|
XP_011526496.1:p.Gly284Arg
|
XM_017027158.1:c.916G>A
|
XP_016882647.1:p.Gly306Arg
|