ENST00000242375.8:c.352A>T
MANE Select
|
ENSP00000242375.3:p.Ile118Phe
|
|
ENST00000242375.7:c.352A>T
|
ENSP00000242375.3:p.Ile118Phe
|
|
ENST00000411726.6:c.352A>T
|
ENSP00000402374.2:p.Ile118Phe
|
|
ENST00000432161.5:c.352A>T
|
ENSP00000389197.1:p.Ile118Phe
|
|
ENST00000438242.1:c.184A>T
|
ENSP00000397042.1:p.Ile62Phe
|
|
ENST00000468877.2:n.262A>T
|
|
|
ENST00000470851.1:n.16A>T
|
|
|
NM_001190906.1:c.352A>T
|
NP_001177835.1:p.Ile118Phe
|
|
NM_001190907.1:c.352A>T
|
NP_001177836.1:p.Ile118Phe
|
|
NM_005989.3:c.352A>T
|
NP_005980.1:p.Ile118Phe
|
|
NM_005989.4:c.352A>T
MANE Select
|
NP_005980.1:p.Ile118Phe
|
|
NM_001190906.2:c.352A>T
|
NP_001177835.1:p.Ile118Phe
|
|
NM_001190907.2:c.352A>T
|
NP_001177836.1:p.Ile118Phe
|
|