|
ENST00000560968.6:c.*533del
(HNF1A)
|
ENSP00000453965.2:n.*533del
|
|
|
ENST00000257555.11:c.1786del
(HNF1A)
MANE Select
|
ENSP00000257555.5:p.Val596CysfsTer?
|
|
|
ENST00000257555.10:c.1786del
(HNF1A)
|
ENSP00000257555.4:p.Val596CysfsTer?
|
|
|
ENST00000288757.7:c.*3072del
(C12orf43)
MANE Select
|
ENSP00000288757.5:n.*3072del
|
|
|
ENST00000540108.1:c.*1226del
(HNF1A)
|
ENSP00000445445.1:n.*1226del
|
|
|
ENST00000541395.5:c.1879del
(HNF1A)
|
ENSP00000443112.1:p.Val627CysfsTer?
|
|
|
ENST00000543427.5:c.1249del
(HNF1A)
|
ENSP00000439721.2:p.Val417CysfsTer?
|
|
|
ENST00000544413.2:c.1807del
(HNF1A)
|
ENSP00000438804.1:p.Val603CysfsTer?
|
|
|
ENST00000560968.5:c.1603del
(HNF1A)
|
|
|
|
ENST00000615446.4:c.574del
(HNF1A)
|
ENSP00000483994.1:p.Val192CysfsTer?
|
|
|
ENST00000617366.4:c.*195del
(HNF1A)
|
ENSP00000481967.1:n.*195del
|
|
|
NM_000545.5:c.1786del , LRG_522t1:c.1786del
(HNF1A)
|
NP_000536.5:p.Val596CysfsTer?
|
|
|
NM_000545.6:c.1786del
(HNF1A)
|
NP_000536.5:p.Val596CysfsTer?
|
|
|
NM_001306179.1:c.1807del
(HNF1A)
|
NP_001293108.1:p.Val603CysfsTer?
|
|
|
XM_005253931.2:c.1879del
(HNF1A)
|
XP_005253988.1:p.Val627CysfsTer?
|
|
|
XM_024449168.1:c.1879del
(HNF1A)
|
XP_024304936.1:p.Val627CysfsTer?
|
|
|
NM_000545.8:c.1786del
(HNF1A)
MANE Select
|
NP_000536.6:p.Val596CysfsTer?
|
|
|
NM_001286191.2:c.*3072del
(C12orf43)
|
NP_001273120.1:n.*3072del
|
|
|
NM_001286196.2:c.*3072del
(C12orf43)
|
NP_001273125.1:n.*3072del
|
|
|
NM_001306179.2:c.1807del
(HNF1A)
|
NP_001293108.2:p.Val603CysfsTer?
|
|
|
NM_022895.3:c.*3072del
(C12orf43)
MANE Select
|
NP_075046.1:n.*3072del
|
|
