ENST00000496887.7:c.725C>T
|
ENSP00000434560.2:p.Ala242Val
|
|
ENST00000646564.2:c.542C>T
|
ENSP00000495806.2:p.Ala181Val
|
|
ENST00000155840.12:c.986C>T
MANE Select
|
ENSP00000155840.2:p.Ala329Val
|
|
ENST00000335475.6:c.605C>T
|
ENSP00000334497.5:p.Ala202Val
|
|
ENST00000646564.1:c.188C>T
|
ENSP00000495806.1:p.Ala63Val
|
|
ENST00000155840.9:c.986C>T
|
ENSP00000155840.2:p.Ala329Val
|
|
ENST00000335475.5:c.605C>T
|
ENSP00000334497.5:p.Ala202Val
|
|
NM_000218.2:c.986C>T , LRG_287t1:c.986C>T
|
NP_000209.2:p.Ala329Val
|
|
NM_181798.1:c.605C>T , LRG_287t2:c.605C>T
|
NP_861463.1:p.Ala202Val
|
|
NM_000218.3:c.986C>T
MANE Select
|
NP_000209.2:p.Ala329Val
|
|