ENST00000255030.9:c.637C>G
MANE Select
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ENSP00000255030.5:p.Gln213Glu
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ENST00000368110.1:c.271C>G
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ENSP00000357091.1:p.Gln91Glu
|
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ENST00000368111.5:c.271C>G
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ENSP00000357092.1:p.Gln91Glu
|
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ENST00000368112.5:c.238C>G
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ENSP00000357093.1:p.Gln80Glu
|
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ENST00000437342.1:c.103C>G
|
ENSP00000402788.1:p.Gln35Glu
|
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ENST00000473196.1:n.205C>G
|
|
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ENST00000489317.1:n.74+444C>G
|
|
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NM_000567.2:c.637C>G
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NP_000558.2:p.Gln213Glu
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XM_011509207.1:c.637C>G
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XP_011507509.1:p.Gln213Glu
|
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NM_001329057.1:c.637C>G
|
NP_001315986.1:p.Gln213Glu
|
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NM_001329058.1:c.238C>G
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NP_001315987.1:p.Gln80Glu
|
|
NM_000567.3:c.637C>G
MANE Select
|
NP_000558.2:p.Gln213Glu
|
|
NM_001329057.2:c.637C>G
|
NP_001315986.1:p.Gln213Glu
|
|
NM_001329058.2:c.238C>G
|
NP_001315987.1:p.Gln80Glu
|
|
NM_001382703.1:c.271C>G
|
NP_001369632.1:p.Gln91Glu
|
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