ENST00000496887.7:c.1412C>T
|
ENSP00000434560.2:p.Ala471Val
|
|
ENST00000646564.2:c.1229C>T
|
ENSP00000495806.2:p.Ala410Val
|
|
ENST00000155840.12:c.1769C>T
MANE Select
|
ENSP00000155840.2:p.Ala590Val
|
|
ENST00000335475.6:c.1388C>T
|
ENSP00000334497.5:p.Ala463Val
|
|
ENST00000526095.2:c.173C>T
|
ENSP00000494939.1:p.Ala58Val
|
|
ENST00000646564.1:c.875C>T
|
ENSP00000495806.1:p.Ala292Val
|
|
ENST00000155840.9:c.1769C>T
|
ENSP00000155840.2:p.Ala590Val
|
|
ENST00000335475.5:c.1388C>T
|
ENSP00000334497.5:p.Ala463Val
|
|
ENST00000526095.1:n.276C>T
|
|
|
NM_000218.2:c.1769C>T , LRG_287t1:c.1769C>T
|
NP_000209.2:p.Ala590Val
|
|
NM_181798.1:c.1388C>T , LRG_287t2:c.1388C>T
|
NP_861463.1:p.Ala463Val
|
|
NM_000218.3:c.1769C>T
MANE Select
|
NP_000209.2:p.Ala590Val
|
|