ENST00000228916.7:c.414C>A
MANE Select
|
ENSP00000228916.2:p.Tyr138Ter
|
|
ENST00000228916.6:c.414C>A
|
ENSP00000228916.2:p.Tyr138Ter
|
|
ENST00000338748.9:c.414C>A
|
ENSP00000345028.5:p.Tyr138Ter
|
|
ENST00000360168.7:c.591C>A
|
ENSP00000353292.3:p.Tyr197Ter
|
|
ENST00000396966.6:c.414C>A
|
ENSP00000380166.2:p.Tyr138Ter
|
|
ENST00000536176.1:n.495C>A
|
|
|
ENST00000536788.1:c.477C>A
|
ENSP00000443434.1:p.Tyr159Ter
|
|
ENST00000538979.5:n.82+983C>A
|
|
|
ENST00000543585.1:n.550C>A
|
|
|
ENST00000543768.1:c.483C>A
|
ENSP00000438739.1:p.Tyr161Ter
|
|
ENST00000544882.1:n.418C>A
|
|
|
NM_001038.5:c.414C>A
|
NP_001029.1:p.Tyr138Ter
|
|
NM_001159575.1:c.483C>A
|
NP_001153047.1:p.Tyr161Ter
|
|
NM_001159576.1:c.591C>A
|
NP_001153048.1:p.Tyr197Ter
|
|
NM_001038.6:c.414C>A
MANE Select
|
NP_001029.1:p.Tyr138Ter
|
|
NM_001159576.2:c.591C>A
|
NP_001153048.1:p.Tyr197Ter
|
|
NM_001159575.2:c.483C>A
|
NP_001153047.1:p.Tyr161Ter
|
|