ENST00000252288.8:c.439C>G
MANE Select
|
ENSP00000252288.1:p.His147Asp
|
|
ENST00000447102.8:c.439C>G
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ENSP00000403536.2:p.His147Asp
|
|
ENST00000591788.3:c.122C>G
|
|
|
ENST00000640164.1:n.272C>G
|
|
|
ENST00000640762.1:c.370C>G
|
ENSP00000492031.1:p.His124Asp
|
|
ENST00000252288.6:c.439C>G
|
ENSP00000252288.1:p.His147Asp
|
|
ENST00000447102.7:c.439C>G
|
ENSP00000403536.2:p.His147Asp
|
|
ENST00000591788.2:c.124C>G
|
ENSP00000466341.2:p.His42Asp
|
|
NM_000156.5:c.439C>G
|
NP_000147.1:p.His147Asp
|
|
NM_138924.2:c.439C>G
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NP_620279.1:p.His147Asp
|
|
NM_000156.6:c.439C>G
MANE Select
|
NP_000147.1:p.His147Asp
|
|
NM_138924.3:c.439C>G
|
NP_620279.1:p.His147Asp
|
|