ENST00000253108.9:c.947+152C>T
(EIF3G)
MANE Select
|
ENSP00000253108.3:n.947+152C>T
|
|
ENST00000321826.5:c.*589G>A
(P2RY11)
MANE Select
|
ENSP00000323872.4:n.*589G>A
|
|
ENST00000253108.8:c.947+152C>T
(EIF3G)
|
ENSP00000253108.3:n.947+152C>T
|
|
ENST00000321826.4:c.*589G>A
(P2RY11)
|
ENSP00000323872.4:n.*589G>A
|
|
ENST00000590158.1:n.966+152C>T
(EIF3G)
|
|
|
ENST00000593054.5:c.341+152C>T
(EIF3G)
|
ENSP00000467187.1:n.341+152C>T
|
|
NM_001040664.2:c.*589G>A
(PPAN-P2RY11)
|
NP_001035754.1:n.*589G>A
|
|
NM_001198690.1:c.*1473G>A
(PPAN-P2RY11)
|
NP_001185619.1:n.*1473G>A
|
|
NM_002566.4:c.*589G>A
(P2RY11)
|
NP_002557.2:n.*589G>A
|
|
NM_003755.3:c.947+152C>T
(EIF3G)
|
NP_003746.2:n.947+152C>T
|
|
NM_003755.4:c.947+152C>T
(EIF3G)
|
NP_003746.2:n.947+152C>T
|
|
NM_002566.5:c.*589G>A
(P2RY11)
MANE Select
|
NP_002557.2:n.*589G>A
|
|
NM_003755.5:c.947+152C>T
(EIF3G)
MANE Select
|
NP_003746.2:n.947+152C>T
|
|
NM_001040664.3:c.*589G>A
(PPAN-P2RY11)
|
NP_001035754.1:n.*589G>A
|
|
NM_001198690.2:c.*1473G>A
(PPAN-P2RY11)
|
NP_001185619.1:n.*1473G>A
|
|