ENST00000682275.1:c.1697_1723del
|
ENSP00000507852.1:p.Leu566_Tyr575delinsHis
|
|
ENST00000683395.1:c.1638_1664del
|
|
|
ENST00000684087.1:c.1661_1687del
|
ENSP00000506978.1:p.Leu554_Tyr563delinsHis
|
|
ENST00000506362.2:c.1412_1438del
|
ENSP00000424103.2:p.Leu471_Tyr480delinsHis
|
|
ENST00000673642.1:c.1320_1346del
|
ENSP00000501242.1:n.1320_1346del
|
|
ENST00000673991.1:c.1697_1723del
|
ENSP00000501033.1:p.Leu566_Tyr575delinsHis
|
|
ENST00000226760.5:c.1661_1687del
MANE Select
|
ENSP00000226760.1:p.Leu554_Tyr563delinsHis
|
|
ENST00000503569.5:c.1661_1687del
|
ENSP00000423337.1:p.Leu554_Tyr563delinsHis
|
|
ENST00000507765.1:n.1846_1872del
|
|
|
NM_001145853.1:c.1661_1687del
|
NP_001139325.1:p.Leu554_Tyr563delinsHis
|
|
NM_006005.3:c.1661_1687del
MANE Select
|
NP_005996.2:p.Leu554_Tyr563delinsHis
|
|
XM_017008586.1:c.1670_1696del
|
XP_016864075.1:p.Leu557_Tyr566delinsHis
|
|