ENST00000309755.9:c.1566C>T
MANE Select
|
ENSP00000312397.4:p.Asp522=
|
|
ENST00000309755.8:c.1566C>T
|
ENSP00000312397.4:p.Asp522=
|
|
ENST00000447439.6:n.1622C>T
|
|
|
ENST00000504208.5:c.*450C>T
|
ENSP00000423585.1:n.*450C>T
|
|
ENST00000506491.5:c.1320C>T
|
ENSP00000424828.1:p.Asp440=
|
|
ENST00000506873.5:n.1089C>T
|
|
|
ENST00000508657.5:c.1470C>T
|
ENSP00000422099.1:p.Asp490=
|
|
ENST00000509694.1:n.359C>T
|
|
|
NM_001257194.1:c.1470C>T
|
NP_001244123.1:p.Asp490=
|
|
NM_001257195.1:c.1320C>T
|
NP_001244124.1:p.Asp440=
|
|
NM_017415.2:c.1566C>T
|
NP_059111.2:p.Asp522=
|
|
NM_017415.3:c.1566C>T
MANE Select
|
NP_059111.2:p.Asp522=
|
|
NM_001257195.2:c.1320C>T
|
NP_001244124.1:p.Asp440=
|
|