ENST00000613132.5:c.*26G=
MANE Select
|
ENSP00000477772.2:n.*26G=
|
|
ENST00000381083.9:c.*26G=
|
ENSP00000370473.4:n.*26G=
|
|
ENST00000275521.10:c.*26G=
|
ENSP00000275521.5:n.*26G=
|
|
ENST00000381083.8:c.*26G=
|
ENSP00000370473.4:n.*26G=
|
|
ENST00000381086.9:c.*26G=
|
ENSP00000370476.4:n.*26G=
|
|
ENST00000460209.1:n.532G=
|
|
|
ENST00000613132.4:c.839G=
|
ENSP00000477772.1:n.839G=
|
|
NM_000598.4:c.*26G=
|
NP_000589.2:n.*26G=
|
|
NM_001013398.1:c.*26G=
|
NP_001013416.1:n.*26G=
|
|
NM_001013398.2:c.*26G=
|
NP_001013416.1:n.*26G=
|
|
NM_000598.5:c.*26G=
MANE Select
|
NP_000589.2:n.*26G=
|
|