ENST00000253122.10:c.1218C>G
MANE Select
|
ENSP00000253122.5:p.Phe406Leu
|
|
ENST00000253122.9:c.1218C>G
|
ENSP00000253122.5:p.Phe406Leu
|
|
ENST00000413787.1:c.258-223C>G
|
ENSP00000400463.1:n.258-223C>G
|
|
ENST00000430077.6:c.873C>G
|
ENSP00000403041.2:p.Phe291Leu
|
|
ENST00000442457.1:c.272C>G
|
|
|
ENST00000457723.1:c.202C>G
|
ENSP00000394742.1:p.Leu68Val
|
|
ENST00000485324.1:n.1251C>G
|
|
|
NM_001142805.1:c.1188C>G
|
NP_001136277.1:p.Phe396Leu
|
|
NM_001142806.1:c.873C>G
|
NP_001136278.1:p.Phe291Leu
|
|
NM_005629.3:c.1218C>G
|
NP_005620.1:p.Phe406Leu
|
|
NM_005629.4:c.1218C>G
MANE Select
|
NP_005620.1:p.Phe406Leu
|
|
NM_001142805.2:c.1188C>G
|
NP_001136277.1:p.Phe396Leu
|
|