ENST00000290866.10:c.1126C>A
MANE Select
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ENSP00000290866.4:p.Gln376Lys
|
|
ENST00000290866.9:c.1126C>A
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ENSP00000290866.4:p.Gln376Lys
|
|
ENST00000428043.5:c.1126C>A
|
ENSP00000397593.2:p.Gln376Lys
|
|
ENST00000582678.5:c.*525C>A
|
ENSP00000462995.1:n.*525C>A
|
|
ENST00000584529.5:n.1160C>A
|
|
|
NM_000789.3:c.1126C>A
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NP_000780.1:p.Gln376Lys
|
|
XM_005257110.1:c.577C>A
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XP_005257167.1:p.Gln193Lys
|
|
NM_000789.4:c.1126C>A
MANE Select
|
NP_000780.1:p.Gln376Lys
|
|
NM_001382700.1:c.559C>A
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NP_001369629.1:p.Gln187Lys
|
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NM_001382701.1:c.274C>A
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NP_001369630.1:p.Gln92Lys
|
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