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NM_006767.4:c.1104C>G
MANE Select
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NP_006758.2:p.Asp368Glu
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ENST00000646124.2:c.1104C>G
MANE Select
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ENSP00000496779.1:p.Asp368Glu
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NM_006767.3:c.1104C>G
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NP_006758.2:p.Asp368Glu
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ENST00000215739.12:c.1104C>G
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ENSP00000215739.8:p.Asp368Glu
|
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ENST00000461510.1:n.205C>G
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|
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ENST00000479606.5:n.1250C>G
|
|
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ENST00000492480.1:n.160C>G
|
|
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ENST00000495142.6:n.449C>G
|
|
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ENST00000497716.5:n.931C>G
|
|
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ENST00000642151.1:c.935C>G
|
|
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ENST00000643578.1:n.1126C>G
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|
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ENST00000646506.1:n.683C>G
|
|
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ENST00000700578.1:c.1104C>G
|
ENSP00000515073.1:p.Asp368Glu
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