ENST00000371696.7:c.*215_*216insTGGGCT
MANE Select
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ENSP00000360761.2:n.*215_*216insTGGGCT
|
|
ENST00000371694.7:c.*215_*216insTGGGCT
|
ENSP00000360759.3:n.*215_*216insTGGGCT
|
|
ENST00000371696.6:c.*215_*216insTGGGCT
|
ENSP00000360761.2:n.*215_*216insTGGGCT
|
|
ENST00000538402.1:c.*215_*216insTGGGCT
|
ENSP00000438919.1:n.*215_*216insTGGGCT
|
|
NM_001012727.1:c.*215_*216insTGGGCT
|
NP_001012745.1:n.*215_*216insTGGGCT
|
|
NM_006412.3:c.*215_*216insTGGGCT
|
NP_006403.2:n.*215_*216insTGGGCT
|
|
NM_006412.4:c.*215_*216insTGGGCT
MANE Select
|
NP_006403.2:n.*215_*216insTGGGCT
|
|
NM_001012727.2:c.*215_*216insTGGGCT
|
NP_001012745.1:n.*215_*216insTGGGCT
|
|