ENST00000253108.9:c.*94C>A
(EIF3G)
MANE Select
|
ENSP00000253108.3:n.*94C>A
|
|
ENST00000321826.5:c.*282G>T
(P2RY11)
MANE Select
|
ENSP00000323872.4:n.*282G>T
|
|
ENST00000253108.8:c.*94C>A
(EIF3G)
|
ENSP00000253108.3:n.*94C>A
|
|
ENST00000321826.4:c.*282G>T
(P2RY11)
|
ENSP00000323872.4:n.*282G>T
|
|
ENST00000593054.5:c.451C>A
(EIF3G)
|
ENSP00000467187.1:n.451C>A
|
|
NM_001040664.2:c.*282G>T
(PPAN-P2RY11)
|
NP_001035754.1:n.*282G>T
|
|
NM_001198690.1:c.*1166G>T
(PPAN-P2RY11)
|
NP_001185619.1:n.*1166G>T
|
|
NM_002566.4:c.*282G>T
(P2RY11)
|
NP_002557.2:n.*282G>T
|
|
NM_003755.3:c.*94C>A
(EIF3G)
|
NP_003746.2:n.*94C>A
|
|
NM_003755.4:c.*94C>A
(EIF3G)
|
NP_003746.2:n.*94C>A
|
|
NM_002566.5:c.*282G>T
(P2RY11)
MANE Select
|
NP_002557.2:n.*282G>T
|
|
NM_003755.5:c.*94C>A
(EIF3G)
MANE Select
|
NP_003746.2:n.*94C>A
|
|
NM_001040664.3:c.*282G>T
(PPAN-P2RY11)
|
NP_001035754.1:n.*282G>T
|
|
NM_001198690.2:c.*1166G>T
(PPAN-P2RY11)
|
NP_001185619.1:n.*1166G>T
|
|