ENST00000631182.3:c.697+139A>G
MANE Plus Clinical
|
ENSP00000486885.1:n.697+139A>G
|
|
ENST00000375437.7:c.649A>G
MANE Select
|
ENSP00000364586.2:p.Arg217Gly
|
|
ENST00000635945.1:n.1012A>G
|
|
|
ENST00000636071.2:c.697+139A>G
|
ENSP00000490107.1:n.697+139A>G
|
|
ENST00000636135.1:c.520A>G
|
ENSP00000489821.1:p.Arg174Gly
|
|
ENST00000636384.2:c.649A>G
|
ENSP00000490765.1:p.Arg217Gly
|
|
ENST00000636662.2:c.*1172A>G
|
ENSP00000489873.1:n.*1172A>G
|
|
ENST00000636769.1:c.649A>G
|
ENSP00000490800.1:p.Arg217Gly
|
|
ENST00000636985.2:c.253A>G
|
ENSP00000490849.1:p.Arg85Gly
|
|
ENST00000637266.2:c.649A>G
|
ENSP00000490866.1:p.Arg217Gly
|
|
ENST00000637367.1:c.*582A>G
|
ENSP00000490592.1:n.*582A>G
|
|
ENST00000638151.1:n.733A>G
|
|
|
ENST00000283256.10:c.649A>G
|
ENSP00000283256.6:p.Arg217Gly
|
|
ENST00000375427.4:c.697+139A>G
|
ENSP00000364576.2:n.697+139A>G
|
|
ENST00000375437.6:c.649A>G
|
ENSP00000364586.2:p.Arg217Gly
|
|
ENST00000424833.5:c.649A>G
|
ENSP00000406454.2:p.Arg217Gly
|
|
ENST00000480032.4:n.792A>G
|
|
|
ENST00000486878.2:c.190A>G
|
ENSP00000487466.1:p.Arg64Gly
|
|
ENST00000631182.2:c.697+139A>G
|
ENSP00000486885.1:n.697+139A>G
|
|
NM_001040142.1:c.649A>G
|
NP_001035232.1:p.Arg217Gly
|
|
NM_001040143.1:c.697+139A>G
|
NP_001035233.1:n.697+139A>G
|
|
NM_021007.2:c.649A>G
|
NP_066287.2:p.Arg217Gly
|
|
XM_005246750.2:c.649A>G
|
XP_005246807.1:p.Arg217Gly
|
|
XM_005246753.2:c.697+139A>G
|
XP_005246810.1:n.697+139A>G
|
|
XM_005246754.3:c.619A>G
|
XP_005246811.1:p.Arg207Gly
|
|
XM_005246755.3:c.-57+601A>G
|
XP_005246812.1:n.-57+601A>G
|
|
XM_011511608.1:c.649A>G
|
XP_011509910.1:p.Arg217Gly
|
|
XM_011511609.1:c.649A>G
|
XP_011509911.1:p.Arg217Gly
|
|
XM_005246753.3:c.697+139A>G
|
XP_005246810.1:n.697+139A>G
|
|
XM_017004656.1:c.649A>G
|
XP_016860145.1:p.Arg217Gly
|
|
XM_017004657.1:c.697+139A>G
|
XP_016860146.1:n.697+139A>G
|
|
XM_017004658.1:c.-105A>G
|
XP_016860147.1:n.-105A>G
|
|
XM_024453037.1:c.-57+601A>G
|
XP_024308805.1:n.-57+601A>G
|
|
NM_001040142.2:c.649A>G
MANE Select
|
NP_001035232.1:p.Arg217Gly
|
|
NM_001040143.2:c.697+139A>G
|
NP_001035233.1:n.697+139A>G
|
|
NM_001371246.1:c.697+139A>G
MANE Plus Clinical
|
NP_001358175.1:n.697+139A>G
|
|
NM_001371247.1:c.649A>G
|
NP_001358176.1:p.Arg217Gly
|
|
NM_021007.3:c.649A>G
|
NP_066287.2:p.Arg217Gly
|
|