|
ENST00000347147.9:c.1119G>T
MANE Select
|
ENSP00000333355.6:p.Arg373=
|
|
|
ENST00000347147.8:c.1119G>T
|
ENSP00000333355.6:p.Arg373=
|
|
|
ENST00000381975.7:c.1115G>T
|
ENSP00000371402.3:p.Gly372Val
|
|
|
ENST00000392432.6:c.1260G>T
|
ENSP00000376227.2:p.Arg420=
|
|
|
ENST00000419280.5:c.*415G>T
|
ENSP00000414077.1:n.*415G>T
|
|
|
ENST00000429560.1:c.311G>T
|
ENSP00000403053.1:p.Gly104Val
|
|
|
ENST00000432352.5:c.393G>T
|
ENSP00000409963.1:p.Arg131=
|
|
|
ENST00000452358.5:c.618G>T
|
ENSP00000414333.1:p.Arg206=
|
|
|
ENST00000467284.1:n.165G>T
|
|
|
|
ENST00000473092.5:c.1119G>T
|
ENSP00000418674.1:p.Arg373=
|
|
|
ENST00000477651.5:n.883G>T
|
|
|
|
NM_001011655.2:c.1119G>T
|
NP_001011655.1:p.Arg373=
|
|
|
NM_001166305.1:c.1260G>T
|
NP_001159777.1:p.Arg420=
|
|
|
NM_001166306.1:c.1115G>T
|
NP_001159778.1:p.Gly372Val
|
|
|
NM_138399.4:c.1119G>T
|
NP_612408.3:p.Arg373=
|
|
|
XM_005269371.3:c.1119G>T
|
XP_005269428.1:p.Arg373=
|
|
|
XM_011513318.1:c.1269G>T
|
XP_011511620.1:p.Arg423=
|
|
|
XM_011513319.1:c.1206G>T
|
XP_011511621.1:p.Arg402=
|
|
|
XM_011513320.1:c.1317G>T
|
XP_011511622.1:p.Arg439=
|
|
|
XM_011513321.1:c.1185G>T
|
XP_011511623.1:p.Arg395=
|
|
|
XM_011513322.1:c.1176G>T
|
XP_011511624.1:p.Arg392=
|
|
|
XM_011513323.1:c.1014G>T
|
XP_011511625.1:p.Arg338=
|
|
|
XM_005269371.4:c.1119G>T
|
XP_005269428.1:p.Arg373=
|
|
|
XM_011513318.2:c.1269G>T
|
XP_011511620.1:p.Arg423=
|
|
|
XM_011513319.2:c.1206G>T
|
XP_011511621.1:p.Arg402=
|
|
|
XM_011513320.2:c.1317G>T
|
XP_011511622.1:p.Arg439=
|
|
|
XM_011513321.2:c.1185G>T
|
XP_011511623.1:p.Arg395=
|
|
|
XM_011513322.2:c.1176G>T
|
XP_011511624.1:p.Arg392=
|
|
|
XM_017007517.1:c.1128G>T
|
XP_016863006.1:p.Arg376=
|
|
|
XM_017007518.1:c.1128G>T
|
XP_016863007.1:p.Arg376=
|
|
|
NM_001011655.3:c.1119G>T
MANE Select
|
NP_001011655.1:p.Arg373=
|
|
|
NM_001166305.2:c.1260G>T
|
NP_001159777.1:p.Arg420=
|
|
|
NM_001166306.2:c.1115G>T
|
NP_001159778.1:p.Gly372Val
|
|
|
NM_138399.5:c.1119G>T
|
NP_612408.3:p.Arg373=
|
|
