ENST00000684241.1:n.3291G=
|
|
|
ENST00000262186.10:c.2458G=
MANE Select
|
ENSP00000262186.5:p.Gly820=
|
|
ENST00000330883.9:c.1438G=
|
ENSP00000328531.4:p.Gly480=
|
|
ENST00000262186.9:c.2458G=
|
ENSP00000262186.5:p.Gly820=
|
|
ENST00000330883.8:c.1438G=
|
ENSP00000328531.4:p.Gly480=
|
|
NM_000238.3:c.2458G= , LRG_288t1:c.2458G=
|
NP_000229.1:p.Gly820=
|
|
NM_172057.2:c.1438G= , LRG_288t3:c.1438G=
|
NP_742054.1:p.Gly480=
|
|
XM_011516185.1:c.2158G=
|
XP_011514487.1:p.Gly720=
|
|
XM_011516186.1:c.2458G=
|
XP_011514488.1:p.Gly820=
|
|
XM_011516185.2:c.2158G=
|
XP_011514487.1:p.Gly720=
|
|
XM_011516186.3:c.2458G=
|
XP_011514488.1:p.Gly820=
|
|
XM_017012195.1:c.2308G=
|
XP_016867684.1:p.Gly770=
|
|
XM_017012196.1:c.2281G=
|
XP_016867685.1:p.Gly761=
|
|
NM_000238.4:c.2458G=
MANE Select
|
NP_000229.1:p.Gly820=
|
|
NM_172057.3:c.1438G=
|
NP_742054.1:p.Gly480=
|
|