ENST00000295897.9:c.1765G>C
MANE Select
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ENSP00000295897.4:p.Glu589Gln
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ENST00000295897.8:c.1765G>C
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ENSP00000295897.4:p.Glu589Gln
|
|
ENST00000401494.7:c.1420G>C
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ENSP00000384695.3:p.Glu474Gln
|
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ENST00000415165.6:c.1189G>C
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ENSP00000401820.2:p.Glu397Gln
|
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ENST00000476441.6:c.*1044G>C
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ENSP00000423727.1:n.*1044G>C
|
|
ENST00000495173.1:n.73G>C
|
|
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ENST00000503124.5:c.1315G>C
|
ENSP00000421027.1:p.Glu439Gln
|
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ENST00000505649.5:n.1312G>C
|
|
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ENST00000508932.5:n.175+164G>C
|
|
|
ENST00000509063.5:c.1765G>C
|
ENSP00000422784.1:p.Glu589Gln
|
|
ENST00000511370.1:c.1298G>C
|
|
|
ENST00000621085.4:c.1126G>C
|
ENSP00000483421.1:p.Glu376Gln
|
|
ENST00000621628.4:c.1126G>C
|
ENSP00000480485.1:p.Glu376Gln
|
|
NM_000477.5:c.1765G>C
|
NP_000468.1:p.Glu589Gln
|
|
NM_000477.6:c.1765G>C
|
NP_000468.1:p.Glu589Gln
|
|
NM_000477.7:c.1765G>C
MANE Select
|
NP_000468.1:p.Glu589Gln
|
|