ENST00000253122.10:c.1209T>C
MANE Select
|
ENSP00000253122.5:p.Ala403=
|
|
ENST00000253122.9:c.1209T>C
|
ENSP00000253122.5:p.Ala403=
|
|
ENST00000413787.1:c.258-232T>C
|
ENSP00000400463.1:n.258-232T>C
|
|
ENST00000430077.6:c.864T>C
|
ENSP00000403041.2:p.Ala288=
|
|
ENST00000442457.1:c.263T>C
|
|
|
ENST00000457723.1:c.193T>C
|
ENSP00000394742.1:p.Cys65Arg
|
|
ENST00000467402.1:n.308T>C
|
|
|
ENST00000485324.1:n.1242T>C
|
|
|
NM_001142805.1:c.1179T>C
|
NP_001136277.1:p.Ala393=
|
|
NM_001142806.1:c.864T>C
|
NP_001136278.1:p.Ala288=
|
|
NM_005629.3:c.1209T>C
|
NP_005620.1:p.Ala403=
|
|
NM_005629.4:c.1209T>C
MANE Select
|
NP_005620.1:p.Ala403=
|
|
NM_001142805.2:c.1179T>C
|
NP_001136277.1:p.Ala393=
|
|