ENST00000260210.5:c.1766+1259_1766+1260delinsGT
MANE Select
|
ENSP00000260210.3:n.1766+1259_1766+1260delinsGT
|
|
ENST00000260210.4:c.1766+1259_1766+1260delinsGT
|
ENSP00000260210.3:n.1766+1259_1766+1260delinsGT
|
|
ENST00000375445.7:c.1364+1259_1364+1260delinsGT
|
ENSP00000364594.3:n.1364+1259_1364+1260delinsGT
|
|
ENST00000419189.1:c.541+1259_541+1260delinsGT
|
|
|
NM_001159736.1:c.1364+1259_1364+1260delinsGT
|
NP_001153208.1:n.1364+1259_1364+1260delinsGT
|
|
NM_032725.3:c.1766+1259_1766+1260delinsGT
|
NP_116114.1:n.1766+1259_1766+1260delinsGT
|
|
XM_011543035.1:c.1667+1259_1667+1260delinsGT
|
XP_011541337.1:n.1667+1259_1667+1260delinsGT
|
|
XM_011543035.2:c.1667+1259_1667+1260delinsGT
|
XP_011541337.1:n.1667+1259_1667+1260delinsGT
|
|
NM_032725.4:c.1766+1259_1766+1260delinsGT
MANE Select
|
NP_116114.1:n.1766+1259_1766+1260delinsGT
|
|
NM_001159736.2:c.1364+1259_1364+1260delinsGT
|
NP_001153208.1:n.1364+1259_1364+1260delinsGT
|
|