ENST00000295897.9:c.1814C>G
MANE Select
|
ENSP00000295897.4:p.Ala605Gly
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ENST00000295897.8:c.1814C>G
|
ENSP00000295897.4:p.Ala605Gly
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|
ENST00000401494.7:c.1469C>G
|
ENSP00000384695.3:p.Ala490Gly
|
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ENST00000415165.6:c.1238C>G
|
ENSP00000401820.2:p.Ala413Gly
|
|
ENST00000476441.6:c.*1093C>G
|
ENSP00000423727.1:n.*1093C>G
|
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ENST00000495173.1:n.122C>G
|
|
|
ENST00000503124.5:c.1364C>G
|
ENSP00000421027.1:p.Ala455Gly
|
|
ENST00000505649.5:n.1361C>G
|
|
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ENST00000508932.5:n.204C>G
|
|
|
ENST00000509063.5:c.1785+643C>G
|
ENSP00000422784.1:n.1785+643C>G
|
|
ENST00000511370.1:c.1347C>G
|
|
|
ENST00000621085.4:c.1175C>G
|
ENSP00000483421.1:p.Ala392Gly
|
|
ENST00000621628.4:c.1175C>G
|
ENSP00000480485.1:p.Ala392Gly
|
|
NM_000477.5:c.1814C>G
|
NP_000468.1:p.Ala605Gly
|
|
NM_000477.6:c.1814C>G
|
NP_000468.1:p.Ala605Gly
|
|
NM_000477.7:c.1814C>G
MANE Select
|
NP_000468.1:p.Ala605Gly
|
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