ENST00000496887.7:c.826T>A
|
ENSP00000434560.2:p.Tyr276Asn
|
|
ENST00000646564.2:c.643T>A
|
ENSP00000495806.2:p.Tyr215Asn
|
|
ENST00000155840.12:c.1183T>A
MANE Select
|
ENSP00000155840.2:p.Tyr395Asn
|
|
ENST00000335475.6:c.802T>A
|
ENSP00000334497.5:p.Tyr268Asn
|
|
ENST00000646564.1:c.289T>A
|
ENSP00000495806.1:p.Tyr97Asn
|
|
ENST00000155840.9:c.1183T>A
|
ENSP00000155840.2:p.Tyr395Asn
|
|
ENST00000335475.5:c.802T>A
|
ENSP00000334497.5:p.Tyr268Asn
|
|
NM_000218.2:c.1183T>A , LRG_287t1:c.1183T>A
|
NP_000209.2:p.Tyr395Asn
|
|
NM_181798.1:c.802T>A , LRG_287t2:c.802T>A
|
NP_861463.1:p.Tyr268Asn
|
|
NM_000218.3:c.1183T>A
MANE Select
|
NP_000209.2:p.Tyr395Asn
|
|