ENST00000374479.4:c.1062G>A
MANE Select
|
ENSP00000363603.3:p.Arg354=
|
|
ENST00000374479.3:c.1062G>A
|
ENSP00000363603.3:p.Arg354=
|
|
NM_000147.4:c.1062G>A
|
NP_000138.2:p.Arg354=
|
|
XM_005245821.1:c.687G>A
|
XP_005245878.1:p.Arg229=
|
|
XM_011541167.1:c.429G>A
|
XP_011539469.1:p.Arg143=
|
|
XM_005245821.3:c.687G>A
|
XP_005245878.1:p.Arg229=
|
|
XM_011541167.3:c.429G>A
|
XP_011539469.1:p.Arg143=
|
|
XM_017000905.2:c.759G>A
|
XP_016856394.1:p.Arg253=
|
|
NM_000147.5:c.1062G>A
MANE Select
|
NP_000138.2:p.Arg354=
|
|
NR_174379.1:n.1240G>A
|
|
|
NR_174380.1:n.1289G>A
|
|
|
NR_174381.1:n.1128G>A
|
|
|
NR_174382.1:n.1525G>A
|
|
|