ENST00000691183.1:c.*485C>G
|
ENSP00000509954.1:n.*485C>G
|
|
ENST00000378842.8:c.897C>G
MANE Select
|
ENSP00000368119.4:p.Gly299=
|
|
ENST00000378842.7:c.897C>G
|
ENSP00000368119.3:p.Gly299=
|
|
ENST00000450095.6:c.570C>G
|
ENSP00000401956.2:p.Gly190=
|
|
ENST00000488412.2:n.153C>G
|
|
|
ENST00000489643.6:n.977C>G
|
|
|
ENST00000554550.5:c.*517C>G
|
ENSP00000451435.1:n.*517C>G
|
|
ENST00000554638.5:n.1369C>G
|
|
|
ENST00000555020.5:n.1358C>G
|
|
|
ENST00000555086.5:n.1004C>G
|
|
|
ENST00000555754.1:n.345C>G
|
|
|
ENST00000556278.1:c.432+618C>G
|
ENSP00000451792.1:n.432+618C>G
|
|
ENST00000557706.5:n.1472C>G
|
|
|
NM_000155.3:c.897C>G
|
NP_000146.2:p.Gly299=
|
|
NM_001258332.1:c.570C>G
|
NP_001245261.1:p.Gly190=
|
|
NM_000155.4:c.897C>G
MANE Select
|
NP_000146.2:p.Gly299=
|
|
NM_001258332.2:c.570C>G
|
NP_001245261.1:p.Gly190=
|
|