ENST00000252288.8:c.507C>G
MANE Select
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ENSP00000252288.1:p.Cys169Trp
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ENST00000447102.8:c.507C>G
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ENSP00000403536.2:p.Cys169Trp
|
|
ENST00000591788.3:c.190C>G
|
|
|
ENST00000640164.1:n.340C>G
|
|
|
ENST00000640762.1:c.438C>G
|
ENSP00000492031.1:p.Cys146Trp
|
|
ENST00000252288.6:c.507C>G
|
ENSP00000252288.1:p.Cys169Trp
|
|
ENST00000447102.7:c.507C>G
|
ENSP00000403536.2:p.Cys169Trp
|
|
ENST00000591788.2:c.192C>G
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ENSP00000466341.2:p.Cys64Trp
|
|
NM_000156.5:c.507C>G
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NP_000147.1:p.Cys169Trp
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|
NM_138924.2:c.507C>G
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NP_620279.1:p.Cys169Trp
|
|
NM_000156.6:c.507C>G
MANE Select
|
NP_000147.1:p.Cys169Trp
|
|
NM_138924.3:c.507C>G
|
NP_620279.1:p.Cys169Trp
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