ENST00000691183.1:c.*531C>G
|
ENSP00000509954.1:n.*531C>G
|
|
ENST00000378842.8:c.943C>G
MANE Select
|
ENSP00000368119.4:p.His315Asp
|
|
ENST00000378842.7:c.943C>G
|
ENSP00000368119.3:p.His315Asp
|
|
ENST00000450095.6:c.616C>G
|
ENSP00000401956.2:p.His206Asp
|
|
ENST00000488412.2:n.527C>G
|
|
|
ENST00000489643.6:n.1351C>G
|
|
|
ENST00000554550.5:c.*563C>G
|
ENSP00000451435.1:n.*563C>G
|
|
ENST00000554638.5:n.1415C>G
|
|
|
ENST00000555020.5:n.1732C>G
|
|
|
ENST00000555754.1:n.391C>G
|
|
|
ENST00000556278.1:c.432+992C>G
|
ENSP00000451792.1:n.432+992C>G
|
|
ENST00000557706.5:n.1518C>G
|
|
|
NM_000155.3:c.943C>G
|
NP_000146.2:p.His315Asp
|
|
NM_001258332.1:c.616C>G
|
NP_001245261.1:p.His206Asp
|
|
NM_000155.4:c.943C>G
MANE Select
|
NP_000146.2:p.His315Asp
|
|
NM_001258332.2:c.616C>G
|
NP_001245261.1:p.His206Asp
|
|