ENST00000380588.5:c.719-1497_719-1496delinsCT
MANE Select
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ENSP00000369962.4:n.719-1497_719-1496delinsCT
|
|
ENST00000380588.4:c.719-1497_719-1496delinsCT
|
ENSP00000369962.4:n.719-1497_719-1496delinsCT
|
|
ENST00000479378.1:n.825-1497_825-1496delinsCT
|
|
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NM_001080444.1:c.719-1497_719-1496delinsCT
|
NP_001073913.1:n.719-1497_719-1496delinsCT
|
|
XM_011529472.1:c.989-1497_989-1496delinsCT
|
XP_011527774.1:n.989-1497_989-1496delinsCT
|
|
XM_011529473.1:c.989-1497_989-1496delinsCT
|
XP_011527775.1:n.989-1497_989-1496delinsCT
|
|
XM_011529472.2:c.989-1497_989-1496delinsCT
|
XP_011527774.1:n.989-1497_989-1496delinsCT
|
|
NM_001080444.2:c.719-1497_719-1496delinsCT
MANE Select
|
NP_001073913.1:n.719-1497_719-1496delinsCT
|
|