ENST00000366930.9:c.644A>T
MANE Select
|
ENSP00000355897.4:p.Asp215Val
|
|
ENST00000366929.4:c.728A>T
|
ENSP00000355896.4:p.Asp243Val
|
|
ENST00000366930.8:c.644A>T
|
ENSP00000355897.4:p.Asp215Val
|
|
ENST00000479322.1:n.128A>T
|
|
|
NM_001135599.2:c.728A>T
|
NP_001129071.1:p.Asp243Val
|
|
NM_003238.3:c.644A>T
|
NP_003229.1:p.Asp215Val
|
|
NM_001135599.3:c.728A>T
|
NP_001129071.1:p.Asp243Val
|
|
NM_003238.4:c.644A>T
|
NP_003229.1:p.Asp215Val
|
|
NR_138148.1:n.2062A>T
|
|
|
NR_138149.1:n.2146A>T
|
|
|
NM_003238.5:c.644A>T
|
NP_003229.1:p.Asp215Val
|
|
NM_003238.6:c.644A>T
MANE Select
|
NP_003229.1:p.Asp215Val
|
|
NM_001135599.4:c.728A>T
|
NP_001129071.1:p.Asp243Val
|
|
NR_138148.2:n.2010A>T
|
|
|
NR_138149.2:n.2094A>T
|
|
|