|
ENST00000686218.1:c.792T>G
|
ENSP00000509288.1:p.Thr264=
|
|
|
ENST00000691144.1:n.3172T>G
|
|
|
|
ENST00000691249.1:n.1781T>G
|
|
|
|
ENST00000442944.7:c.939T>G
|
ENSP00000392041.3:p.Thr313=
|
|
|
ENST00000640813.1:c.*194T>G
|
ENSP00000491061.1:n.*194T>G
|
|
|
ENST00000648026.1:c.851T>G
|
ENSP00000498044.1:n.851T>G
|
|
|
ENST00000648374.1:c.906T>G
|
ENSP00000497255.1:p.Thr302=
|
|
|
ENST00000650101.1:c.888T>G
|
ENSP00000496970.1:p.Thr296=
|
|
|
ENST00000650307.1:n.1783T>G
|
|
|
|
ENST00000652429.1:c.957T>G
MANE Select
|
ENSP00000498786.1:p.Thr319=
|
|
|
ENST00000278715.7:c.957T>G
|
ENSP00000278715.3:p.Thr319=
|
|
|
ENST00000392841.1:c.906T>G
|
ENSP00000376584.1:p.Thr302=
|
|
|
ENST00000442944.6:c.906T>G
|
ENSP00000392041.2:p.Thr302=
|
|
|
ENST00000537841.5:c.906T>G
|
ENSP00000444730.1:p.Thr302=
|
|
|
ENST00000539045.1:n.456T>G
|
|
|
|
ENST00000542044.5:n.1402T>G
|
|
|
|
ENST00000542729.5:c.786T>G
|
ENSP00000443058.1:p.Thr262=
|
|
|
ENST00000543090.5:c.864T>G
|
ENSP00000445429.1:p.Thr288=
|
|
|
ENST00000543543.5:n.1432T>G
|
|
|
|
ENST00000544182.1:n.1406T>G
|
|
|
|
ENST00000544387.5:c.837T>G
|
ENSP00000438424.1:p.Thr279=
|
|
|
ENST00000546226.5:n.1719T>G
|
|
|
|
NM_000190.3:c.957T>G
|
NP_000181.2:p.Thr319=
|
|
|
NM_001024382.1:c.906T>G
|
NP_001019553.1:p.Thr302=
|
|
|
NM_001258208.1:c.837T>G
|
NP_001245137.1:p.Thr279=
|
|
|
NM_001258209.1:c.786T>G
|
NP_001245138.1:p.Thr262=
|
|
|
XM_005271531.1:c.906T>G
|
XP_005271588.1:p.Thr302=
|
|
|
XM_005271532.1:c.906T>G
|
XP_005271589.1:p.Thr302=
|
|
|
XM_005271533.2:c.903T>G
|
XP_005271590.1:p.Thr301=
|
|
|
XM_011542796.1:c.792T>G
|
XP_011541098.1:p.Thr264=
|
|
|
NM_000190.4:c.957T>G
MANE Select
|
NP_000181.2:p.Thr319=
|
|
|
NM_001024382.2:c.906T>G
|
NP_001019553.1:p.Thr302=
|
|
|
XM_005271533.3:c.903T>G
|
XP_005271590.1:p.Thr301=
|
|
|
XM_017017629.1:c.906T>G
|
XP_016873118.1:p.Thr302=
|
|
|
XM_024448460.1:c.783T>G
|
XP_024304228.1:p.Thr261=
|
|
|
NM_001258208.2:c.837T>G
|
NP_001245137.1:p.Thr279=
|
|
|
NM_001258209.2:c.786T>G
|
NP_001245138.1:p.Thr262=
|
|
