ENST00000290866.10:c.314A=
MANE Select
|
ENSP00000290866.4:p.Tyr105=
|
|
ENST00000290866.9:c.314A=
|
ENSP00000290866.4:p.Tyr105=
|
|
ENST00000428043.5:c.314A=
|
ENSP00000397593.2:p.Tyr105=
|
|
ENST00000579462.1:n.339A=
|
|
|
ENST00000580318.1:n.503A=
|
|
|
ENST00000582627.1:c.314A=
|
ENSP00000462280.1:p.Tyr105=
|
|
ENST00000582678.5:c.314A=
|
ENSP00000462995.1:p.Tyr105=
|
|
ENST00000583336.5:n.348A=
|
|
|
ENST00000584529.5:n.348A=
|
|
|
NM_000789.3:c.314A=
|
NP_000780.1:p.Tyr105=
|
|
XM_005257110.1:c.-142A=
|
XP_005257167.1:n.-142A=
|
|
NM_000789.4:c.314A=
MANE Select
|
NP_000780.1:p.Tyr105=
|
|
NM_001382700.1:c.79A=
|
NP_001369629.1:p.Met27=
|
|
NM_001382701.1:c.-301A=
|
NP_001369630.1:n.-301A=
|
|