ENST00000253122.10:c.1194G>T
MANE Select
|
ENSP00000253122.5:p.Val398=
|
|
ENST00000253122.9:c.1194G>T
|
ENSP00000253122.5:p.Val398=
|
|
ENST00000413787.1:c.258-247G>T
|
ENSP00000400463.1:n.258-247G>T
|
|
ENST00000430077.6:c.849G>T
|
ENSP00000403041.2:p.Val283=
|
|
ENST00000442457.1:c.248G>T
|
|
|
ENST00000457723.1:c.178G>T
|
ENSP00000394742.1:p.Gly60Cys
|
|
ENST00000467402.1:n.293G>T
|
|
|
ENST00000485324.1:n.1227G>T
|
|
|
NM_001142805.1:c.1164G>T
|
NP_001136277.1:p.Val388=
|
|
NM_001142806.1:c.849G>T
|
NP_001136278.1:p.Val283=
|
|
NM_005629.3:c.1194G>T
|
NP_005620.1:p.Val398=
|
|
NM_005629.4:c.1194G>T
MANE Select
|
NP_005620.1:p.Val398=
|
|
NM_001142805.2:c.1164G>T
|
NP_001136277.1:p.Val388=
|
|