ENST00000560968.6:c.*1081G>C
(HNF1A)
|
ENSP00000453965.2:n.*1081G>C
|
|
ENST00000257555.11:c.*438G>C
(HNF1A)
MANE Select
|
ENSP00000257555.5:n.*438G>C
|
|
ENST00000257555.10:c.*438G>C
(HNF1A)
|
ENSP00000257555.4:n.*438G>C
|
|
ENST00000288757.7:c.*2523C>G
(C12orf43)
MANE Select
|
ENSP00000288757.5:n.*2523C>G
|
|
ENST00000540108.1:c.*1774G>C
(HNF1A)
|
ENSP00000445445.1:n.*1774G>C
|
|
ENST00000541395.5:c.*438G>C
(HNF1A)
|
ENSP00000443112.1:n.*438G>C
|
|
ENST00000543427.5:c.*438G>C
(HNF1A)
|
ENSP00000439721.2:n.*438G>C
|
|
ENST00000560968.5:c.2151G>C
(HNF1A)
|
|
|
ENST00000615446.4:c.*438G>C
(HNF1A)
|
ENSP00000483994.1:n.*438G>C
|
|
ENST00000617366.4:c.*743G>C
(HNF1A)
|
ENSP00000481967.1:n.*743G>C
|
|
NM_000545.5:c.*438G>C , LRG_522t1:c.*438G>C
(HNF1A)
|
NP_000536.5:n.*438G>C
|
|
NM_000545.6:c.*438G>C
(HNF1A)
|
NP_000536.5:n.*438G>C
|
|
NM_001306179.1:c.*438G>C
(HNF1A)
|
NP_001293108.1:n.*438G>C
|
|
XM_005253931.2:c.*438G>C
(HNF1A)
|
XP_005253988.1:n.*438G>C
|
|
XM_024449168.1:c.*438G>C
(HNF1A)
|
XP_024304936.1:n.*438G>C
|
|
NM_000545.8:c.*438G>C
(HNF1A)
MANE Select
|
NP_000536.6:n.*438G>C
|
|
NM_001286191.2:c.*2523C>G
(C12orf43)
|
NP_001273120.1:n.*2523C>G
|
|
NM_001286196.2:c.*2523C>G
(C12orf43)
|
NP_001273125.1:n.*2523C>G
|
|
NM_001306179.2:c.*438G>C
(HNF1A)
|
NP_001293108.2:n.*438G>C
|
|
NM_022895.3:c.*2523C>G
(C12orf43)
MANE Select
|
NP_075046.1:n.*2523C>G
|
|