ENST00000253108.9:c.*99T>C
(EIF3G)
MANE Select
|
ENSP00000253108.3:n.*99T>C
|
|
ENST00000321826.5:c.*277A>G
(P2RY11)
MANE Select
|
ENSP00000323872.4:n.*277A>G
|
|
ENST00000321826.4:c.*277A>G
(P2RY11)
|
ENSP00000323872.4:n.*277A>G
|
|
NM_001040664.2:c.*277A>G
(PPAN-P2RY11)
|
NP_001035754.1:n.*277A>G
|
|
NM_001198690.1:c.*1161A>G
(PPAN-P2RY11)
|
NP_001185619.1:n.*1161A>G
|
|
NM_002566.4:c.*277A>G
(P2RY11)
|
NP_002557.2:n.*277A>G
|
|
NM_003755.3:c.*99T>C
(EIF3G)
|
NP_003746.2:n.*99T>C
|
|
NM_003755.4:c.*99T>C
(EIF3G)
|
NP_003746.2:n.*99T>C
|
|
NM_002566.5:c.*277A>G
(P2RY11)
MANE Select
|
NP_002557.2:n.*277A>G
|
|
NM_003755.5:c.*99T>C
(EIF3G)
MANE Select
|
NP_003746.2:n.*99T>C
|
|
NM_001040664.3:c.*277A>G
(PPAN-P2RY11)
|
NP_001035754.1:n.*277A>G
|
|
NM_001198690.2:c.*1161A>G
(PPAN-P2RY11)
|
NP_001185619.1:n.*1161A>G
|
|