ENST00000290866.10:c.1122C>T
MANE Select
|
ENSP00000290866.4:p.Ile374=
|
|
ENST00000290866.9:c.1122C>T
|
ENSP00000290866.4:p.Ile374=
|
|
ENST00000428043.5:c.1122C>T
|
ENSP00000397593.2:p.Ile374=
|
|
ENST00000582678.5:c.*521C>T
|
ENSP00000462995.1:n.*521C>T
|
|
ENST00000584529.5:n.1156C>T
|
|
|
NM_000789.3:c.1122C>T
|
NP_000780.1:p.Ile374=
|
|
XM_005257110.1:c.573C>T
|
XP_005257167.1:p.Ile191=
|
|
NM_000789.4:c.1122C>T
MANE Select
|
NP_000780.1:p.Ile374=
|
|
NM_001382700.1:c.555C>T
|
NP_001369629.1:p.Ile185=
|
|
NM_001382701.1:c.270C>T
|
NP_001369630.1:p.Ile90=
|
|