ENST00000295897.9:c.1814C>A
MANE Select
|
ENSP00000295897.4:p.Ala605Asp
|
|
ENST00000295897.8:c.1814C>A
|
ENSP00000295897.4:p.Ala605Asp
|
|
ENST00000401494.7:c.1469C>A
|
ENSP00000384695.3:p.Ala490Asp
|
|
ENST00000415165.6:c.1238C>A
|
ENSP00000401820.2:p.Ala413Asp
|
|
ENST00000476441.6:c.*1093C>A
|
ENSP00000423727.1:n.*1093C>A
|
|
ENST00000495173.1:n.122C>A
|
|
|
ENST00000503124.5:c.1364C>A
|
ENSP00000421027.1:p.Ala455Asp
|
|
ENST00000505649.5:n.1361C>A
|
|
|
ENST00000508932.5:n.204C>A
|
|
|
ENST00000509063.5:c.1785+643C>A
|
ENSP00000422784.1:n.1785+643C>A
|
|
ENST00000511370.1:c.1347C>A
|
|
|
ENST00000621085.4:c.1175C>A
|
ENSP00000483421.1:p.Ala392Asp
|
|
ENST00000621628.4:c.1175C>A
|
ENSP00000480485.1:p.Ala392Asp
|
|
NM_000477.5:c.1814C>A
|
NP_000468.1:p.Ala605Asp
|
|
NM_000477.6:c.1814C>A
|
NP_000468.1:p.Ala605Asp
|
|
NM_000477.7:c.1814C>A
MANE Select
|
NP_000468.1:p.Ala605Asp
|
|