|
NM_003590.5:c.1636C>T
MANE Select
|
NP_003581.1:p.Arg546Ter
|
|
ENST00000264414.9:c.1636C>T
MANE Select
|
ENSP00000264414.4:p.Arg546Ter
|
|
NM_001257197.1:c.1438C>T
|
NP_001244126.1:p.Arg480Ter
|
|
NM_001257197.2:c.1438C>T
|
NP_001244126.1:p.Arg480Ter
|
|
NM_001257198.1:c.1654C>T
|
NP_001244127.1:p.Arg552Ter
|
|
NM_001257198.2:c.1654C>T
|
NP_001244127.1:p.Arg552Ter
|
|
NM_003590.4:c.1636C>T
|
NP_003581.1:p.Arg546Ter
|
|
ENST00000264414.8:c.1636C>T
|
ENSP00000264414.4:p.Arg546Ter
|
|
ENST00000344951.8:c.1438C>T
|
ENSP00000343601.4:p.Arg480Ter
|
|
ENST00000409096.5:c.1564C>T
|
ENSP00000387200.1:p.Arg522Ter
|
|
ENST00000409777.5:c.1564C>T
|
ENSP00000386525.1:p.Arg522Ter
|
|
ENST00000487558.1:n.61C>T
|
|
|
ENST00000617432.4:c.358C>T
|
ENSP00000477851.1:p.Arg120Ter
|
|
XM_006712800.2:c.1603C>T
|
XP_006712863.2:p.Arg535Ter
|
|
XM_011511994.1:c.1489C>T
|
XP_011510296.1:p.Arg497Ter
|
|
XM_011511994.3:c.1489C>T
|
XP_011510296.1:p.Arg497Ter
|
|
XM_011511995.1:c.1594C>T
|
XP_011510297.1:p.Arg532Ter
|
|
XM_011511996.1:c.1444C>T
|
XP_011510298.1:p.Arg482Ter
|
|
XM_011511996.2:c.1444C>T
|
XP_011510298.1:p.Arg482Ter
|
|
XM_011511997.1:c.1336C>T
|
XP_011510299.1:p.Arg446Ter
|