ENST00000302804.12:c.682C>T
MANE Select
|
ENSP00000302898.6:p.Leu228Phe
|
|
ENST00000302804.11:c.682C>T
|
ENSP00000302898.6:p.Leu228Phe
|
|
ENST00000415300.6:c.625C>T
|
ENSP00000407162.1:p.Leu209Phe
|
|
ENST00000448930.5:c.577C>T
|
ENSP00000406798.2:p.Leu193Phe
|
|
ENST00000594599.1:c.166C>T
|
ENSP00000469894.1:p.Leu56Phe
|
|
ENST00000596375.1:c.*243C>T
|
ENSP00000470465.1:n.*243C>T
|
|
ENST00000598785.5:c.580C>T
|
ENSP00000471830.1:p.Leu194Phe
|
|
ENST00000599062.5:c.673C>T
|
ENSP00000469983.1:p.Leu225Phe
|
|
ENST00000601799.5:c.*981C>T
|
ENSP00000468918.1:n.*981C>T
|
|
NM_001015878.1:c.682C>T
|
NP_001015878.1:p.Leu228Phe
|
|
NM_001015879.1:c.625C>T
|
NP_001015879.1:p.Leu209Phe
|
|
NM_003160.2:c.580C>T
|
NP_003151.2:p.Leu194Phe
|
|
XR_430209.2:n.1576C>T
|
|
|
XR_430209.3:n.1619C>T
|
|
|
NM_001015878.2:c.682C>T
MANE Select
|
NP_001015878.1:p.Leu228Phe
|
|
NM_001015879.2:c.625C>T
|
NP_001015879.1:p.Leu209Phe
|
|
NM_003160.3:c.580C>T
|
NP_003151.2:p.Leu194Phe
|
|