ENST00000258145.8:c.1111A>C
MANE Select
|
ENSP00000258145.3:p.Asn371His
|
|
ENST00000258145.7:c.1111A>C
|
ENSP00000258145.3:p.Asn371His
|
|
ENST00000418919.6:c.943A>C
|
ENSP00000413130.2:p.Asn315His
|
|
ENST00000537823.1:n.110A>C
|
|
|
ENST00000540196.5:c.557-5932A>C
|
|
|
ENST00000540883.1:n.174A>C
|
|
|
ENST00000541781.5:n.1166A>C
|
|
|
ENST00000542058.5:c.1051A>C
|
ENSP00000444819.1:p.Asn351His
|
|
ENST00000543646.5:c.1207A>C
|
ENSP00000438497.1:p.Asn403His
|
|
NM_002076.3:c.1111A>C
|
NP_002067.1:p.Asn371His
|
|
NM_002076.4:c.1111A>C
MANE Select
|
NP_002067.1:p.Asn371His
|
|