ENST00000347404.10:c.169T>A
|
ENSP00000054216.5:p.Tyr57Asn
|
|
ENST00000644744.1:c.169T>A
MANE Select
|
ENSP00000495951.1:p.Tyr57Asn
|
|
ENST00000646633.1:c.*170T>A
|
ENSP00000494139.1:n.*170T>A
|
|
ENST00000228280.9:c.169T>A
|
ENSP00000228280.5:p.Tyr57Asn
|
|
ENST00000347404.9:c.169T>A
|
ENSP00000054216.5:p.Tyr57Asn
|
|
ENST00000357116.4:c.-47-25327T>A
|
ENSP00000474021.1:n.-47-25327T>A
|
|
ENST00000378535.4:n.112T>A
|
|
|
ENST00000552044.1:c.16T>A
|
ENSP00000475042.1:p.Tyr6Asn
|
|
NM_000899.4:c.169T>A
|
NP_000890.1:p.Tyr57Asn
|
|
NM_003994.5:c.169T>A
|
NP_003985.2:p.Tyr57Asn
|
|
NM_000899.5:c.169T>A
MANE Select
|
NP_000890.1:p.Tyr57Asn
|
|
NM_003994.6:c.169T>A
|
NP_003985.2:p.Tyr57Asn
|
|