ENST00000355832.10:c.3802C>G
MANE Select
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ENSP00000348089.5:p.His1268Asp
|
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ENST00000679552.1:n.873C>G
|
|
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ENST00000679871.1:n.948C>G
|
|
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ENST00000679974.1:n.851C>G
|
|
|
ENST00000681632.1:n.5205C>G
|
|
|
ENST00000681659.1:c.3643C>G
|
ENSP00000505631.1:p.His1215Asp
|
|
ENST00000355832.9:c.3802C>G
|
ENSP00000348089.5:p.His1268Asp
|
|
ENST00000465653.1:n.124C>G
|
|
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ENST00000623073.3:c.*2098C>G
|
ENSP00000485650.1:n.*2098C>G
|
|
ENST00000623115.3:c.1912C>G
|
ENSP00000485321.1:p.His638Asp
|
|
ENST00000624341.3:c.1634C>G
|
|
|
NM_000124.3:c.3802C>G
|
NP_000115.1:p.His1268Asp
|
|
XR_945953.1:n.243-10032G>C
|
|
|
NM_001346440.1:c.3802C>G
|
NP_001333369.1:p.His1268Asp
|
|
NM_000124.4:c.3802C>G
MANE Select
|
NP_000115.1:p.His1268Asp
|
|
NM_001346440.2:c.3802C>G
|
NP_001333369.1:p.His1268Asp
|
|