ENST00000682275.1:c.1694_1695insTCAT
|
ENSP00000507852.1:p.Leu566HisfsTer?
|
|
ENST00000683395.1:c.1635_1636insTCAT
|
|
|
ENST00000684087.1:c.1658_1659insTCAT
|
ENSP00000506978.1:p.Leu554HisfsTer?
|
|
ENST00000506362.2:c.1409_1410insTCAT
|
ENSP00000424103.2:p.Leu471HisfsTer?
|
|
ENST00000673642.1:c.1317_1318insTCAT
|
ENSP00000501242.1:n.1317_1318insTCAT
|
|
ENST00000673991.1:c.1694_1695insTCAT
|
ENSP00000501033.1:p.Leu566HisfsTer?
|
|
ENST00000226760.5:c.1658_1659insTCAT
MANE Select
|
ENSP00000226760.1:p.Leu554HisfsTer?
|
|
ENST00000503569.5:c.1658_1659insTCAT
|
ENSP00000423337.1:p.Leu554HisfsTer?
|
|
ENST00000507765.1:n.1843_1844insTCAT
|
|
|
NM_001145853.1:c.1658_1659insTCAT
|
NP_001139325.1:p.Leu554HisfsTer?
|
|
NM_006005.3:c.1658_1659insTCAT
MANE Select
|
NP_005996.2:p.Leu554HisfsTer?
|
|
XM_017008586.1:c.1667_1668insTCAT
|
XP_016864075.1:p.Leu557HisfsTer?
|
|