ENST00000686218.1:c.694G>T
|
ENSP00000509288.1:p.Gly232Cys
|
|
ENST00000691144.1:n.3074G>T
|
|
|
ENST00000691249.1:n.1683G>T
|
|
|
ENST00000442944.7:c.841G>T
|
ENSP00000392041.3:p.Gly281Cys
|
|
ENST00000640813.1:c.*96G>T
|
ENSP00000491061.1:n.*96G>T
|
|
ENST00000648026.1:c.753G>T
|
ENSP00000498044.1:n.753G>T
|
|
ENST00000648374.1:c.808G>T
|
ENSP00000497255.1:p.Gly270Cys
|
|
ENST00000650101.1:c.790G>T
|
ENSP00000496970.1:p.Gly264Cys
|
|
ENST00000650307.1:n.1685G>T
|
|
|
ENST00000652429.1:c.859G>T
MANE Select
|
ENSP00000498786.1:p.Gly287Cys
|
|
ENST00000278715.7:c.859G>T
|
ENSP00000278715.3:p.Gly287Cys
|
|
ENST00000392841.1:c.808G>T
|
ENSP00000376584.1:p.Gly270Cys
|
|
ENST00000442944.6:c.808G>T
|
ENSP00000392041.2:p.Gly270Cys
|
|
ENST00000537841.5:c.808G>T
|
ENSP00000444730.1:p.Gly270Cys
|
|
ENST00000539045.1:n.358G>T
|
|
|
ENST00000542044.5:n.1304G>T
|
|
|
ENST00000542729.5:c.688G>T
|
ENSP00000443058.1:p.Gly230Cys
|
|
ENST00000543090.5:c.766G>T
|
ENSP00000445429.1:p.Gly256Cys
|
|
ENST00000543543.5:n.1334G>T
|
|
|
ENST00000544182.1:n.1308G>T
|
|
|
ENST00000544387.5:c.739G>T
|
ENSP00000438424.1:p.Gly247Cys
|
|
ENST00000546226.5:n.1621G>T
|
|
|
NM_000190.3:c.859G>T
|
NP_000181.2:p.Gly287Cys
|
|
NM_001024382.1:c.808G>T
|
NP_001019553.1:p.Gly270Cys
|
|
NM_001258208.1:c.739G>T
|
NP_001245137.1:p.Gly247Cys
|
|
NM_001258209.1:c.688G>T
|
NP_001245138.1:p.Gly230Cys
|
|
XM_005271531.1:c.808G>T
|
XP_005271588.1:p.Gly270Cys
|
|
XM_005271532.1:c.808G>T
|
XP_005271589.1:p.Gly270Cys
|
|
XM_005271533.2:c.805G>T
|
XP_005271590.1:p.Gly269Cys
|
|
XM_011542796.1:c.694G>T
|
XP_011541098.1:p.Gly232Cys
|
|
NM_000190.4:c.859G>T
MANE Select
|
NP_000181.2:p.Gly287Cys
|
|
NM_001024382.2:c.808G>T
|
NP_001019553.1:p.Gly270Cys
|
|
XM_005271533.3:c.805G>T
|
XP_005271590.1:p.Gly269Cys
|
|
XM_017017629.1:c.808G>T
|
XP_016873118.1:p.Gly270Cys
|
|
XM_024448460.1:c.685G>T
|
XP_024304228.1:p.Gly229Cys
|
|
NM_001258208.2:c.739G>T
|
NP_001245137.1:p.Gly247Cys
|
|
NM_001258209.2:c.688G>T
|
NP_001245138.1:p.Gly230Cys
|
|