ENST00000686218.1:c.454C>G
|
ENSP00000509288.1:p.His152Asp
|
|
ENST00000691144.1:n.2360C>G
|
|
|
ENST00000691249.1:n.1203C>G
|
|
|
ENST00000442944.7:c.601C>G
|
ENSP00000392041.3:p.His201Asp
|
|
ENST00000536813.6:c.568C>G
|
ENSP00000438726.2:p.His190Asp
|
|
ENST00000546302.6:c.541C>G
|
ENSP00000445599.1:p.His181Asp
|
|
ENST00000640813.1:c.461+257C>G
|
ENSP00000491061.1:n.461+257C>G
|
|
ENST00000648026.1:c.513C>G
|
ENSP00000498044.1:p.Cys171Trp
|
|
ENST00000648374.1:c.568C>G
|
ENSP00000497255.1:p.His190Asp
|
|
ENST00000648488.1:c.*92C>G
|
ENSP00000498079.1:n.*92C>G
|
|
ENST00000649823.1:n.836C>G
|
|
|
ENST00000650101.1:c.550C>G
|
ENSP00000496970.1:p.His184Asp
|
|
ENST00000650307.1:n.1445C>G
|
|
|
ENST00000652429.1:c.619C>G
MANE Select
|
ENSP00000498786.1:p.His207Asp
|
|
ENST00000278715.7:c.619C>G
|
ENSP00000278715.3:p.His207Asp
|
|
ENST00000392841.1:c.568C>G
|
ENSP00000376584.1:p.His190Asp
|
|
ENST00000442944.6:c.568C>G
|
ENSP00000392041.2:p.His190Asp
|
|
ENST00000537841.5:c.568C>G
|
ENSP00000444730.1:p.His190Asp
|
|
ENST00000542044.5:n.1064C>G
|
|
|
ENST00000542345.5:n.757C>G
|
|
|
ENST00000542729.5:c.568C>G
|
ENSP00000443058.1:p.His190Asp
|
|
ENST00000543090.5:c.559-273C>G
|
ENSP00000445429.1:n.559-273C>G
|
|
ENST00000543543.5:n.854C>G
|
|
|
ENST00000544182.1:n.594C>G
|
|
|
ENST00000544387.5:c.619C>G
|
ENSP00000438424.1:p.His207Asp
|
|
ENST00000545621.5:c.*514C>G
|
ENSP00000444849.1:n.*514C>G
|
|
ENST00000546226.5:n.907C>G
|
|
|
ENST00000546302.5:c.541C>G
|
ENSP00000445599.1:p.His181Asp
|
|
NM_000190.3:c.619C>G
|
NP_000181.2:p.His207Asp
|
|
NM_001024382.1:c.568C>G
|
NP_001019553.1:p.His190Asp
|
|
NM_001258208.1:c.619C>G
|
NP_001245137.1:p.His207Asp
|
|
NM_001258209.1:c.568C>G
|
NP_001245138.1:p.His190Asp
|
|
XM_005271531.1:c.568C>G
|
XP_005271588.1:p.His190Asp
|
|
XM_005271532.1:c.568C>G
|
XP_005271589.1:p.His190Asp
|
|
XM_005271533.2:c.565C>G
|
XP_005271590.1:p.His189Asp
|
|
XM_011542796.1:c.454C>G
|
XP_011541098.1:p.His152Asp
|
|
NM_000190.4:c.619C>G
MANE Select
|
NP_000181.2:p.His207Asp
|
|
NM_001024382.2:c.568C>G
|
NP_001019553.1:p.His190Asp
|
|
XM_005271533.3:c.565C>G
|
XP_005271590.1:p.His189Asp
|
|
XM_017017629.1:c.568C>G
|
XP_016873118.1:p.His190Asp
|
|
XM_024448460.1:c.565C>G
|
XP_024304228.1:p.His189Asp
|
|
NM_001258208.2:c.619C>G
|
NP_001245137.1:p.His207Asp
|
|
NM_001258209.2:c.568C>G
|
NP_001245138.1:p.His190Asp
|
|