ENST00000496887.7:c.733T>G
|
ENSP00000434560.2:p.Phe245Val
|
|
ENST00000646564.2:c.550T>G
|
ENSP00000495806.2:p.Phe184Val
|
|
ENST00000155840.12:c.994T>G
MANE Select
|
ENSP00000155840.2:p.Phe332Val
|
|
ENST00000335475.6:c.613T>G
|
ENSP00000334497.5:p.Phe205Val
|
|
ENST00000646564.1:c.196T>G
|
ENSP00000495806.1:p.Phe66Val
|
|
ENST00000155840.9:c.994T>G
|
ENSP00000155840.2:p.Phe332Val
|
|
ENST00000335475.5:c.613T>G
|
ENSP00000334497.5:p.Phe205Val
|
|
NM_000218.2:c.994T>G , LRG_287t1:c.994T>G
|
NP_000209.2:p.Phe332Val
|
|
NM_181798.1:c.613T>G , LRG_287t2:c.613T>G
|
NP_861463.1:p.Phe205Val
|
|
NM_000218.3:c.994T>G
MANE Select
|
NP_000209.2:p.Phe332Val
|
|