ENST00000205402.10:c.860dup
MANE Select
|
ENSP00000205402.3:p.Ile289AsnfsTer2
|
|
ENST00000205402.9:c.860dup
|
ENSP00000205402.3:p.Ile289AsnfsTer2
|
|
ENST00000415325.5:c.*534dup
|
ENSP00000402593.1:n.*534dup
|
|
ENST00000417551.5:c.860dup
|
ENSP00000390667.1:p.Ile289AsnfsTer2
|
|
ENST00000437604.6:c.716dup
|
ENSP00000387542.2:p.Ile241AsnfsTer2
|
|
ENST00000440410.5:c.791dup
|
ENSP00000417016.1:p.Ile266AsnfsTer2
|
|
NM_000108.4:c.860dup
|
NP_000099.2:p.Ile289AsnfsTer2
|
|
NM_001289750.1:c.563dup
|
NP_001276679.1:p.Ile190AsnfsTer2
|
|
NM_001289751.1:c.791dup
|
NP_001276680.1:p.Ile266AsnfsTer2
|
|
NM_001289752.1:c.716dup
|
NP_001276681.1:p.Ile241AsnfsTer2
|
|
NM_000108.5:c.860dup
MANE Select
|
NP_000099.2:p.Ile289AsnfsTer2
|
|