ENST00000290866.10:c.1295A>C
MANE Select
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ENSP00000290866.4:p.Glu432Ala
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ENST00000290866.9:c.1295A>C
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ENSP00000290866.4:p.Glu432Ala
|
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ENST00000428043.5:c.1295A>C
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ENSP00000397593.2:p.Glu432Ala
|
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ENST00000582678.5:c.*694A>C
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ENSP00000462995.1:n.*694A>C
|
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ENST00000584529.5:n.1329A>C
|
|
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NM_000789.3:c.1295A>C
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NP_000780.1:p.Glu432Ala
|
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XM_005257110.1:c.746A>C
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XP_005257167.1:p.Glu249Ala
|
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NM_000789.4:c.1295A>C
MANE Select
|
NP_000780.1:p.Glu432Ala
|
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NM_001382700.1:c.728A>C
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NP_001369629.1:p.Glu243Ala
|
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NM_001382701.1:c.443A>C
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NP_001369630.1:p.Glu148Ala
|
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