ENST00000496887.7:c.682T>G
|
ENSP00000434560.2:p.Tyr228Asp
|
|
ENST00000646564.2:c.499T>G
|
ENSP00000495806.2:p.Tyr167Asp
|
|
ENST00000155840.12:c.943T>G
MANE Select
|
ENSP00000155840.2:p.Tyr315Asp
|
|
ENST00000335475.6:c.562T>G
|
ENSP00000334497.5:p.Tyr188Asp
|
|
ENST00000646564.1:c.145T>G
|
ENSP00000495806.1:p.Tyr49Asp
|
|
ENST00000155840.9:c.943T>G
|
ENSP00000155840.2:p.Tyr315Asp
|
|
ENST00000335475.5:c.562T>G
|
ENSP00000334497.5:p.Tyr188Asp
|
|
NM_000218.2:c.943T>G , LRG_287t1:c.943T>G
|
NP_000209.2:p.Tyr315Asp
|
|
NM_181798.1:c.562T>G , LRG_287t2:c.562T>G
|
NP_861463.1:p.Tyr188Asp
|
|
NM_000218.3:c.943T>G
MANE Select
|
NP_000209.2:p.Tyr315Asp
|
|