NM_000147.5:c.857A=
MANE Select
|
NP_000138.2:p.Gln286=
|
ENST00000374479.4:c.857A=
MANE Select
|
ENSP00000363603.3:p.Gln286=
|
NM_000147.4:c.857A=
|
NP_000138.2:p.Gln286=
|
NR_174379.1:n.1035A=
|
|
NR_174380.1:n.1084A=
|
|
NR_174381.1:n.923A=
|
|
NR_174382.1:n.1320A=
|
|
ENST00000374479.3:c.857A=
|
ENSP00000363603.3:p.Gln286=
|
XM_005245821.1:c.482A=
|
XP_005245878.1:p.Gln161=
|
XM_005245821.3:c.482A=
|
XP_005245878.1:p.Gln161=
|
XM_011541167.1:c.224A=
|
XP_011539469.1:p.Gln75=
|
XM_011541167.3:c.224A=
|
XP_011539469.1:p.Gln75=
|
XM_017000905.2:c.554A=
|
XP_016856394.1:p.Gln185=
|