ENST00000686218.1:c.695G>T
|
ENSP00000509288.1:p.Gly232Val
|
|
ENST00000691144.1:n.3075G>T
|
|
|
ENST00000691249.1:n.1684G>T
|
|
|
ENST00000442944.7:c.842G>T
|
ENSP00000392041.3:p.Gly281Val
|
|
ENST00000640813.1:c.*97G>T
|
ENSP00000491061.1:n.*97G>T
|
|
ENST00000648026.1:c.754G>T
|
ENSP00000498044.1:n.754G>T
|
|
ENST00000648374.1:c.809G>T
|
ENSP00000497255.1:p.Gly270Val
|
|
ENST00000650101.1:c.791G>T
|
ENSP00000496970.1:p.Gly264Val
|
|
ENST00000650307.1:n.1686G>T
|
|
|
ENST00000652429.1:c.860G>T
MANE Select
|
ENSP00000498786.1:p.Gly287Val
|
|
ENST00000278715.7:c.860G>T
|
ENSP00000278715.3:p.Gly287Val
|
|
ENST00000392841.1:c.809G>T
|
ENSP00000376584.1:p.Gly270Val
|
|
ENST00000442944.6:c.809G>T
|
ENSP00000392041.2:p.Gly270Val
|
|
ENST00000537841.5:c.809G>T
|
ENSP00000444730.1:p.Gly270Val
|
|
ENST00000539045.1:n.359G>T
|
|
|
ENST00000542044.5:n.1305G>T
|
|
|
ENST00000542729.5:c.689G>T
|
ENSP00000443058.1:p.Gly230Val
|
|
ENST00000543090.5:c.767G>T
|
ENSP00000445429.1:p.Gly256Val
|
|
ENST00000543543.5:n.1335G>T
|
|
|
ENST00000544182.1:n.1309G>T
|
|
|
ENST00000544387.5:c.740G>T
|
ENSP00000438424.1:p.Gly247Val
|
|
ENST00000546226.5:n.1622G>T
|
|
|
NM_000190.3:c.860G>T
|
NP_000181.2:p.Gly287Val
|
|
NM_001024382.1:c.809G>T
|
NP_001019553.1:p.Gly270Val
|
|
NM_001258208.1:c.740G>T
|
NP_001245137.1:p.Gly247Val
|
|
NM_001258209.1:c.689G>T
|
NP_001245138.1:p.Gly230Val
|
|
XM_005271531.1:c.809G>T
|
XP_005271588.1:p.Gly270Val
|
|
XM_005271532.1:c.809G>T
|
XP_005271589.1:p.Gly270Val
|
|
XM_005271533.2:c.806G>T
|
XP_005271590.1:p.Gly269Val
|
|
XM_011542796.1:c.695G>T
|
XP_011541098.1:p.Gly232Val
|
|
NM_000190.4:c.860G>T
MANE Select
|
NP_000181.2:p.Gly287Val
|
|
NM_001024382.2:c.809G>T
|
NP_001019553.1:p.Gly270Val
|
|
XM_005271533.3:c.806G>T
|
XP_005271590.1:p.Gly269Val
|
|
XM_017017629.1:c.809G>T
|
XP_016873118.1:p.Gly270Val
|
|
XM_024448460.1:c.686G>T
|
XP_024304228.1:p.Gly229Val
|
|
NM_001258208.2:c.740G>T
|
NP_001245137.1:p.Gly247Val
|
|
NM_001258209.2:c.689G>T
|
NP_001245138.1:p.Gly230Val
|
|