ENST00000481739.2:c.337C>T
MANE Select
|
ENSP00000419692.1:p.Leu113Phe
|
|
ENST00000672570.1:c.256C>T
|
ENSP00000500402.1:p.Leu86Phe
|
|
ENST00000356384.4:n.747C>T
|
|
|
ENST00000481739.1:c.337C>T
|
ENSP00000419692.1:p.Leu113Phe
|
|
NM_001291920.1:c.256C>T
|
NP_001278849.1:p.Leu86Phe
|
|
NM_001291921.1:c.46C>T
|
NP_001278850.1:p.Leu16Phe
|
|
NM_002957.5:c.337C>T
|
NP_002948.1:p.Leu113Phe
|
|
NM_002957.6:c.337C>T
MANE Select
|
NP_002948.1:p.Leu113Phe
|
|
NM_001291921.2:c.46C>T
|
NP_001278850.1:p.Leu16Phe
|
|
NM_001291920.2:c.256C>T
|
NP_001278849.1:p.Leu86Phe
|
|