ENST00000295897.9:c.1766A>G
MANE Select
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ENSP00000295897.4:p.Glu589Gly
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ENST00000295897.8:c.1766A>G
|
ENSP00000295897.4:p.Glu589Gly
|
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ENST00000401494.7:c.1421A>G
|
ENSP00000384695.3:p.Glu474Gly
|
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ENST00000415165.6:c.1190A>G
|
ENSP00000401820.2:p.Glu397Gly
|
|
ENST00000476441.6:c.*1045A>G
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ENSP00000423727.1:n.*1045A>G
|
|
ENST00000495173.1:n.74A>G
|
|
|
ENST00000503124.5:c.1316A>G
|
ENSP00000421027.1:p.Glu439Gly
|
|
ENST00000505649.5:n.1313A>G
|
|
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ENST00000508932.5:n.175+165A>G
|
|
|
ENST00000509063.5:c.1766A>G
|
ENSP00000422784.1:p.Glu589Gly
|
|
ENST00000511370.1:c.1299A>G
|
|
|
ENST00000621085.4:c.1127A>G
|
ENSP00000483421.1:p.Glu376Gly
|
|
ENST00000621628.4:c.1127A>G
|
ENSP00000480485.1:p.Glu376Gly
|
|
NM_000477.5:c.1766A>G
|
NP_000468.1:p.Glu589Gly
|
|
NM_000477.6:c.1766A>G
|
NP_000468.1:p.Glu589Gly
|
|
NM_000477.7:c.1766A>G
MANE Select
|
NP_000468.1:p.Glu589Gly
|
|