ENST00000461280.2:n.823G>T
|
|
|
ENST00000684116.1:n.418G>T
|
|
|
ENST00000684241.1:n.2358G>T
|
|
|
ENST00000262186.10:c.1525G>T
MANE Select
|
ENSP00000262186.5:p.Asp509Tyr
|
|
ENST00000330883.9:c.505G>T
|
ENSP00000328531.4:p.Asp169Tyr
|
|
ENST00000262186.9:c.1525G>T
|
ENSP00000262186.5:p.Asp509Tyr
|
|
ENST00000330883.8:c.505G>T
|
ENSP00000328531.4:p.Asp169Tyr
|
|
ENST00000430723.4:c.1177G>T
|
ENSP00000387657.4:p.Asp393Tyr
|
|
ENST00000461280.1:n.812G>T
|
|
|
ENST00000473610.5:n.830G>T
|
|
|
ENST00000532957.5:n.1748G>T
|
|
|
NM_000238.3:c.1525G>T , LRG_288t1:c.1525G>T
|
NP_000229.1:p.Asp509Tyr
|
|
NM_001204798.1:c.505G>T
|
NP_001191727.1:p.Asp169Tyr
|
|
NM_172056.2:c.1525G>T , LRG_288t2:c.1525G>T
|
NP_742053.1:p.Asp509Tyr
|
|
NM_172057.2:c.505G>T , LRG_288t3:c.505G>T
|
NP_742054.1:p.Asp169Tyr
|
|
XM_011516185.1:c.1225G>T
|
XP_011514487.1:p.Asp409Tyr
|
|
XM_011516186.1:c.1525G>T
|
XP_011514488.1:p.Asp509Tyr
|
|
XM_011516185.2:c.1225G>T
|
XP_011514487.1:p.Asp409Tyr
|
|
XM_011516186.3:c.1525G>T
|
XP_011514488.1:p.Asp509Tyr
|
|
XM_017012195.1:c.1375G>T
|
XP_016867684.1:p.Asp459Tyr
|
|
XM_017012196.1:c.1348G>T
|
XP_016867685.1:p.Asp450Tyr
|
|
NM_000238.4:c.1525G>T
MANE Select
|
NP_000229.1:p.Asp509Tyr
|
|
NM_001204798.2:c.505G>T
|
NP_001191727.1:p.Asp169Tyr
|
|
NM_172057.3:c.505G>T
|
NP_742054.1:p.Asp169Tyr
|
|