ENST00000309755.9:c.1521T>G
MANE Select
|
ENSP00000312397.4:p.Val507=
|
|
ENST00000309755.8:c.1521T>G
|
ENSP00000312397.4:p.Val507=
|
|
ENST00000447439.6:n.1577T>G
|
|
|
ENST00000504208.5:c.*405T>G
|
ENSP00000423585.1:n.*405T>G
|
|
ENST00000506491.5:c.1275T>G
|
ENSP00000424828.1:p.Val425=
|
|
ENST00000506873.5:n.1044T>G
|
|
|
ENST00000508657.5:c.1425T>G
|
ENSP00000422099.1:p.Val475=
|
|
ENST00000509694.1:n.314T>G
|
|
|
NM_001257194.1:c.1425T>G
|
NP_001244123.1:p.Val475=
|
|
NM_001257195.1:c.1275T>G
|
NP_001244124.1:p.Val425=
|
|
NM_017415.2:c.1521T>G
|
NP_059111.2:p.Val507=
|
|
NM_017415.3:c.1521T>G
MANE Select
|
NP_059111.2:p.Val507=
|
|
NM_001257195.2:c.1275T>G
|
NP_001244124.1:p.Val425=
|
|