ENST00000253122.10:c.1177G>T
MANE Select
|
ENSP00000253122.5:p.Val393Phe
|
|
ENST00000253122.9:c.1177G>T
|
ENSP00000253122.5:p.Val393Phe
|
|
ENST00000413787.1:c.258-264G>T
|
ENSP00000400463.1:n.258-264G>T
|
|
ENST00000430077.6:c.832G>T
|
ENSP00000403041.2:p.Val278Phe
|
|
ENST00000442457.1:c.231G>T
|
|
|
ENST00000457723.1:c.161G>T
|
ENSP00000394742.1:p.Cys54Phe
|
|
ENST00000467402.1:n.276G>T
|
|
|
ENST00000485324.1:n.1210G>T
|
|
|
NM_001142805.1:c.1147G>T
|
NP_001136277.1:p.Val383Phe
|
|
NM_001142806.1:c.832G>T
|
NP_001136278.1:p.Val278Phe
|
|
NM_005629.3:c.1177G>T
|
NP_005620.1:p.Val393Phe
|
|
NM_005629.4:c.1177G>T
MANE Select
|
NP_005620.1:p.Val393Phe
|
|
NM_001142805.2:c.1147G>T
|
NP_001136277.1:p.Val383Phe
|
|