NM_020706.2:c.1450C>T
MANE Select
|
NP_065757.1:p.Arg484Ter
|
ENST00000286835.12:c.1450C>T
MANE Select
|
ENSP00000286835.7:p.Arg484Ter
|
NM_001145444.1:c.1405C>T
|
NP_001138916.1:p.Arg469Ter
|
NM_001145445.1:c.1450C>T
|
NP_001138917.1:p.Arg484Ter
|
ENST00000286835.11:c.1450C>T
|
ENSP00000286835.7:p.Arg484Ter
|
ENST00000399804.5:c.1450C>T
|
ENSP00000382703.1:p.Arg484Ter
|
ENST00000434667.3:c.1405C>T
|
ENSP00000402377.2:p.Arg469Ter
|
ENST00000467731.1:n.884C>T
|
|
XM_005261017.1:c.1273C>T
|
XP_005261074.1:p.Arg425Ter
|
XM_005261017.3:c.1273C>T
|
XP_005261074.1:p.Arg425Ter
|
XM_006724035.1:c.1438C>T
|
XP_006724098.1:p.Arg480Ter
|
XM_006724035.3:c.1438C>T
|
XP_006724098.1:p.Arg480Ter
|
XM_006724036.1:c.1438C>T
|
XP_006724099.1:p.Arg480Ter
|
XM_006724036.3:c.1438C>T
|
XP_006724099.1:p.Arg480Ter
|
XM_017028415.2:c.1447C>T
|
XP_016883904.1:p.Arg483Ter
|
XM_017028416.2:c.1447C>T
|
XP_016883905.1:p.Arg483Ter
|
XM_017028417.1:c.1273C>T
|
XP_016883906.1:p.Arg425Ter
|