ENST00000368476.4:c.*313_*314del
MANE Select
|
ENSP00000357461.3:n.*313_*314del
|
|
ENST00000636034.1:c.1505+317_1505+318del
|
ENSP00000489703.1:n.1505+317_1505+318del
|
|
ENST00000637900.1:c.*313_*314del
|
ENSP00000490474.1:n.*313_*314del
|
|
ENST00000368476.3:c.*313_*314del
|
ENSP00000357461.3:n.*313_*314del
|
|
NM_000748.2:c.*313_*314del
|
NP_000739.1:n.*313_*314del
|
|
XM_017000180.2:c.*313_*314del
|
XP_016855669.1:n.*313_*314del
|
|
XR_001736952.2:n.2074_2075del
|
|
|
NM_000748.3:c.*313_*314del
MANE Select
|
NP_000739.1:n.*313_*314del
|
|