ENST00000496887.7:c.771+1695A>T
|
ENSP00000434560.2:n.771+1695A>T
|
|
ENST00000646564.2:c.588+1695A>T
|
ENSP00000495806.2:n.588+1695A>T
|
|
ENST00000155840.12:c.1061A>T
MANE Select
|
ENSP00000155840.2:p.Lys354Met
|
|
ENST00000335475.6:c.680A>T
|
ENSP00000334497.5:p.Lys227Met
|
|
ENST00000646564.1:c.234+1695A>T
|
ENSP00000495806.1:n.234+1695A>T
|
|
ENST00000155840.9:c.1061A>T
|
ENSP00000155840.2:p.Lys354Met
|
|
ENST00000335475.5:c.680A>T
|
ENSP00000334497.5:p.Lys227Met
|
|
NM_000218.2:c.1061A>T , LRG_287t1:c.1061A>T
|
NP_000209.2:p.Lys354Met
|
|
NM_181798.1:c.680A>T , LRG_287t2:c.680A>T
|
NP_861463.1:p.Lys227Met
|
|
NM_000218.3:c.1061A>T
MANE Select
|
NP_000209.2:p.Lys354Met
|
|