ENST00000295897.9:c.1814C=
MANE Select
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ENSP00000295897.4:p.Ala605=
|
|
ENST00000295897.8:c.1814C=
|
ENSP00000295897.4:p.Ala605=
|
|
ENST00000401494.7:c.1469C=
|
ENSP00000384695.3:p.Ala490=
|
|
ENST00000415165.6:c.1238C=
|
ENSP00000401820.2:p.Ala413=
|
|
ENST00000476441.6:c.*1093C=
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ENSP00000423727.1:n.*1093C=
|
|
ENST00000495173.1:n.122C=
|
|
|
ENST00000503124.5:c.1364C=
|
ENSP00000421027.1:p.Ala455=
|
|
ENST00000505649.5:n.1361C=
|
|
|
ENST00000508932.5:n.204C=
|
|
|
ENST00000509063.5:c.1785+643C=
|
ENSP00000422784.1:n.1785+643C=
|
|
ENST00000511370.1:c.1347C=
|
|
|
ENST00000621085.4:c.1175C=
|
ENSP00000483421.1:p.Ala392=
|
|
ENST00000621628.4:c.1175C=
|
ENSP00000480485.1:p.Ala392=
|
|
NM_000477.5:c.1814C=
|
NP_000468.1:p.Ala605=
|
|
NM_000477.6:c.1814C=
|
NP_000468.1:p.Ala605=
|
|
NM_000477.7:c.1814C=
MANE Select
|
NP_000468.1:p.Ala605=
|
|