ENST00000461280.2:n.1304G=
|
|
|
ENST00000683359.1:n.130G=
|
|
|
ENST00000684241.1:n.2839G=
|
|
|
ENST00000262186.10:c.2006G=
MANE Select
|
ENSP00000262186.5:p.Gly669=
|
|
ENST00000330883.9:c.986G=
|
ENSP00000328531.4:p.Gly329=
|
|
ENST00000262186.9:c.2006G=
|
ENSP00000262186.5:p.Gly669=
|
|
ENST00000330883.8:c.986G=
|
ENSP00000328531.4:p.Gly329=
|
|
ENST00000430723.4:c.1658G=
|
ENSP00000387657.4:p.Gly553=
|
|
ENST00000461280.1:n.1293G=
|
|
|
ENST00000473610.5:n.1638G=
|
|
|
ENST00000532957.5:n.2229G=
|
|
|
NM_000238.3:c.2006G= , LRG_288t1:c.2006G=
|
NP_000229.1:p.Gly669=
|
|
NM_001204798.1:c.986G=
|
NP_001191727.1:p.Gly329=
|
|
NM_172056.2:c.2006G= , LRG_288t2:c.2006G=
|
NP_742053.1:p.Gly669=
|
|
NM_172057.2:c.986G= , LRG_288t3:c.986G=
|
NP_742054.1:p.Gly329=
|
|
XM_011516185.1:c.1706G=
|
XP_011514487.1:p.Gly569=
|
|
XM_011516186.1:c.2006G=
|
XP_011514488.1:p.Gly669=
|
|
XM_011516185.2:c.1706G=
|
XP_011514487.1:p.Gly569=
|
|
XM_011516186.3:c.2006G=
|
XP_011514488.1:p.Gly669=
|
|
XM_017012195.1:c.1856G=
|
XP_016867684.1:p.Gly619=
|
|
XM_017012196.1:c.1829G=
|
XP_016867685.1:p.Gly610=
|
|
NM_000238.4:c.2006G=
MANE Select
|
NP_000229.1:p.Gly669=
|
|
NM_001204798.2:c.986G=
|
NP_001191727.1:p.Gly329=
|
|
NM_172057.3:c.986G=
|
NP_742054.1:p.Gly329=
|
|