ENST00000560968.6:c.*606C>T
(HNF1A)
|
ENSP00000453965.2:n.*606C>T
|
|
ENST00000257555.11:c.1859C>T
(HNF1A)
MANE Select
|
ENSP00000257555.5:p.Thr620Ile
|
|
ENST00000257555.10:c.1859C>T
(HNF1A)
|
ENSP00000257555.4:p.Thr620Ile
|
|
ENST00000288757.7:c.*2998G>A
(C12orf43)
MANE Select
|
ENSP00000288757.5:n.*2998G>A
|
|
ENST00000540108.1:c.*1299C>T
(HNF1A)
|
ENSP00000445445.1:n.*1299C>T
|
|
ENST00000541395.5:c.1952C>T
(HNF1A)
|
ENSP00000443112.1:p.Thr651Ile
|
|
ENST00000543427.5:c.1322C>T
(HNF1A)
|
ENSP00000439721.2:p.Thr441Ile
|
|
ENST00000544413.2:c.1880C>T
(HNF1A)
|
ENSP00000438804.1:p.Thr627Ile
|
|
ENST00000560968.5:c.1676C>T
(HNF1A)
|
|
|
ENST00000615446.4:c.647C>T
(HNF1A)
|
ENSP00000483994.1:p.Thr216Ile
|
|
ENST00000617366.4:c.*268C>T
(HNF1A)
|
ENSP00000481967.1:n.*268C>T
|
|
NM_000545.5:c.1859C>T , LRG_522t1:c.1859C>T
(HNF1A)
|
NP_000536.5:p.Thr620Ile
|
|
NM_000545.6:c.1859C>T
(HNF1A)
|
NP_000536.5:p.Thr620Ile
|
|
NM_001306179.1:c.1880C>T
(HNF1A)
|
NP_001293108.1:p.Thr627Ile
|
|
XM_005253931.2:c.1952C>T
(HNF1A)
|
XP_005253988.1:p.Thr651Ile
|
|
XM_024449168.1:c.1952C>T
(HNF1A)
|
XP_024304936.1:p.Thr651Ile
|
|
NM_000545.8:c.1859C>T
(HNF1A)
MANE Select
|
NP_000536.6:p.Thr620Ile
|
|
NM_001286191.2:c.*2998G>A
(C12orf43)
|
NP_001273120.1:n.*2998G>A
|
|
NM_001286196.2:c.*2998G>A
(C12orf43)
|
NP_001273125.1:n.*2998G>A
|
|
NM_001306179.2:c.1880C>T
(HNF1A)
|
NP_001293108.2:p.Thr627Ile
|
|
NM_022895.3:c.*2998G>A
(C12orf43)
MANE Select
|
NP_075046.1:n.*2998G>A
|
|