ENST00000264414.9:c.1359C>T
MANE Select
|
ENSP00000264414.4:p.Asn453=
|
|
ENST00000264414.8:c.1359C>T
|
ENSP00000264414.4:p.Asn453=
|
|
ENST00000344951.8:c.1161C>T
|
ENSP00000343601.4:p.Asn387=
|
|
ENST00000409096.5:c.1287C>T
|
ENSP00000387200.1:p.Asn429=
|
|
ENST00000409777.5:c.1287C>T
|
ENSP00000386525.1:p.Asn429=
|
|
ENST00000481135.1:n.655C>T
|
|
|
ENST00000617432.4:c.81C>T
|
ENSP00000477851.1:p.Asn27=
|
|
NM_001257197.1:c.1161C>T
|
NP_001244126.1:p.Asn387=
|
|
NM_001257198.1:c.1377C>T
|
NP_001244127.1:p.Asn459=
|
|
NM_003590.4:c.1359C>T
|
NP_003581.1:p.Asn453=
|
|
XM_006712800.2:c.1326C>T
|
XP_006712863.2:p.Asn442=
|
|
XM_011511994.1:c.1212C>T
|
XP_011510296.1:p.Asn404=
|
|
XM_011511995.1:c.1317C>T
|
XP_011510297.1:p.Asn439=
|
|
XM_011511996.1:c.1167C>T
|
XP_011510298.1:p.Asn389=
|
|
XM_011511997.1:c.1059C>T
|
XP_011510299.1:p.Asn353=
|
|
XM_011511994.3:c.1212C>T
|
XP_011510296.1:p.Asn404=
|
|
XM_011511996.2:c.1167C>T
|
XP_011510298.1:p.Asn389=
|
|
NM_003590.5:c.1359C>T
MANE Select
|
NP_003581.1:p.Asn453=
|
|
NM_001257198.2:c.1377C>T
|
NP_001244127.1:p.Asn459=
|
|
NM_001257197.2:c.1161C>T
|
NP_001244126.1:p.Asn387=
|
|