ENST00000496887.7:c.748A>G
|
ENSP00000434560.2:p.Ile250Val
|
|
ENST00000646564.2:c.565A>G
|
ENSP00000495806.2:p.Ile189Val
|
|
ENST00000155840.12:c.1009A>G
MANE Select
|
ENSP00000155840.2:p.Ile337Val
|
|
ENST00000335475.6:c.628A>G
|
ENSP00000334497.5:p.Ile210Val
|
|
ENST00000646564.1:c.211A>G
|
ENSP00000495806.1:p.Ile71Val
|
|
ENST00000155840.9:c.1009A>G
|
ENSP00000155840.2:p.Ile337Val
|
|
ENST00000335475.5:c.628A>G
|
ENSP00000334497.5:p.Ile210Val
|
|
NM_000218.2:c.1009A>G , LRG_287t1:c.1009A>G
|
NP_000209.2:p.Ile337Val
|
|
NM_181798.1:c.628A>G , LRG_287t2:c.628A>G
|
NP_861463.1:p.Ile210Val
|
|
NM_000218.3:c.1009A>G
MANE Select
|
NP_000209.2:p.Ile337Val
|
|