ENST00000691183.1:c.*532A>G
|
ENSP00000509954.1:n.*532A>G
|
|
ENST00000378842.8:c.944A>G
MANE Select
|
ENSP00000368119.4:p.His315Arg
|
|
ENST00000378842.7:c.944A>G
|
ENSP00000368119.3:p.His315Arg
|
|
ENST00000450095.6:c.617A>G
|
ENSP00000401956.2:p.His206Arg
|
|
ENST00000488412.2:n.528A>G
|
|
|
ENST00000489643.6:n.1352A>G
|
|
|
ENST00000554550.5:c.*564A>G
|
ENSP00000451435.1:n.*564A>G
|
|
ENST00000554638.5:n.1416A>G
|
|
|
ENST00000555020.5:n.1733A>G
|
|
|
ENST00000555754.1:n.392A>G
|
|
|
ENST00000556278.1:c.432+993A>G
|
ENSP00000451792.1:n.432+993A>G
|
|
ENST00000557706.5:n.1519A>G
|
|
|
NM_000155.3:c.944A>G
|
NP_000146.2:p.His315Arg
|
|
NM_001258332.1:c.617A>G
|
NP_001245261.1:p.His206Arg
|
|
NM_000155.4:c.944A>G
MANE Select
|
NP_000146.2:p.His315Arg
|
|
NM_001258332.2:c.617A>G
|
NP_001245261.1:p.His206Arg
|
|