ENST00000684241.1:n.3579G=
|
|
|
ENST00000262186.10:c.2746G=
MANE Select
|
ENSP00000262186.5:p.Gly916=
|
|
ENST00000330883.9:c.1726G=
|
ENSP00000328531.4:p.Gly576=
|
|
ENST00000262186.9:c.2746G=
|
ENSP00000262186.5:p.Gly916=
|
|
ENST00000330883.8:c.1726G=
|
ENSP00000328531.4:p.Gly576=
|
|
NM_000238.3:c.2746G= , LRG_288t1:c.2746G=
|
NP_000229.1:p.Gly916=
|
|
NM_172057.2:c.1726G= , LRG_288t3:c.1726G=
|
NP_742054.1:p.Gly576=
|
|
XM_011516185.1:c.2446G=
|
XP_011514487.1:p.Gly816=
|
|
XM_011516186.1:c.2693-134G=
|
XP_011514488.1:n.2693-134G=
|
|
XM_011516185.2:c.2446G=
|
XP_011514487.1:p.Gly816=
|
|
XM_011516186.3:c.2693-134G=
|
XP_011514488.1:n.2693-134G=
|
|
XM_017012195.1:c.2596G=
|
XP_016867684.1:p.Gly866=
|
|
XM_017012196.1:c.2569G=
|
XP_016867685.1:p.Gly857=
|
|
NM_000238.4:c.2746G=
MANE Select
|
NP_000229.1:p.Gly916=
|
|
NM_172057.3:c.1726G=
|
NP_742054.1:p.Gly576=
|
|