ENST00000253108.9:c.948-140G>T
(EIF3G)
MANE Select
|
ENSP00000253108.3:n.948-140G>T
|
|
ENST00000321826.5:c.*531C>A
(P2RY11)
MANE Select
|
ENSP00000323872.4:n.*531C>A
|
|
ENST00000253108.8:c.948-140G>T
(EIF3G)
|
ENSP00000253108.3:n.948-140G>T
|
|
ENST00000321826.4:c.*531C>A
(P2RY11)
|
ENSP00000323872.4:n.*531C>A
|
|
ENST00000590158.1:n.967-140G>T
(EIF3G)
|
|
|
ENST00000593054.5:c.342-140G>T
(EIF3G)
|
ENSP00000467187.1:n.342-140G>T
|
|
NM_001040664.2:c.*531C>A
(PPAN-P2RY11)
|
NP_001035754.1:n.*531C>A
|
|
NM_001198690.1:c.*1415C>A
(PPAN-P2RY11)
|
NP_001185619.1:n.*1415C>A
|
|
NM_002566.4:c.*531C>A
(P2RY11)
|
NP_002557.2:n.*531C>A
|
|
NM_003755.3:c.948-140G>T
(EIF3G)
|
NP_003746.2:n.948-140G>T
|
|
NM_003755.4:c.948-140G>T
(EIF3G)
|
NP_003746.2:n.948-140G>T
|
|
NM_002566.5:c.*531C>A
(P2RY11)
MANE Select
|
NP_002557.2:n.*531C>A
|
|
NM_003755.5:c.948-140G>T
(EIF3G)
MANE Select
|
NP_003746.2:n.948-140G>T
|
|
NM_001040664.3:c.*531C>A
(PPAN-P2RY11)
|
NP_001035754.1:n.*531C>A
|
|
NM_001198690.2:c.*1415C>A
(PPAN-P2RY11)
|
NP_001185619.1:n.*1415C>A
|
|