ENST00000461280.2:n.1130A=
|
|
|
ENST00000684241.1:n.2665A=
|
|
|
ENST00000262186.10:c.1832A=
MANE Select
|
ENSP00000262186.5:p.Tyr611=
|
|
ENST00000330883.9:c.812A=
|
ENSP00000328531.4:p.Tyr271=
|
|
ENST00000262186.9:c.1832A=
|
ENSP00000262186.5:p.Tyr611=
|
|
ENST00000330883.8:c.812A=
|
ENSP00000328531.4:p.Tyr271=
|
|
ENST00000430723.4:c.1484A=
|
ENSP00000387657.4:p.Tyr495=
|
|
ENST00000461280.1:n.1119A=
|
|
|
ENST00000473610.5:n.1137A=
|
|
|
ENST00000532957.5:n.2055A=
|
|
|
NM_000238.3:c.1832A= , LRG_288t1:c.1832A=
|
NP_000229.1:p.Tyr611=
|
|
NM_001204798.1:c.812A=
|
NP_001191727.1:p.Tyr271=
|
|
NM_172056.2:c.1832A= , LRG_288t2:c.1832A=
|
NP_742053.1:p.Tyr611=
|
|
NM_172057.2:c.812A= , LRG_288t3:c.812A=
|
NP_742054.1:p.Tyr271=
|
|
XM_011516185.1:c.1532A=
|
XP_011514487.1:p.Tyr511=
|
|
XM_011516186.1:c.1832A=
|
XP_011514488.1:p.Tyr611=
|
|
XM_011516185.2:c.1532A=
|
XP_011514487.1:p.Tyr511=
|
|
XM_011516186.3:c.1832A=
|
XP_011514488.1:p.Tyr611=
|
|
XM_017012195.1:c.1682A=
|
XP_016867684.1:p.Tyr561=
|
|
XM_017012196.1:c.1655A=
|
XP_016867685.1:p.Tyr552=
|
|
NM_000238.4:c.1832A=
MANE Select
|
NP_000229.1:p.Tyr611=
|
|
NM_001204798.2:c.812A=
|
NP_001191727.1:p.Tyr271=
|
|
NM_172057.3:c.812A=
|
NP_742054.1:p.Tyr271=
|
|