ENST00000691183.1:c.*463C>G
|
ENSP00000509954.1:n.*463C>G
|
|
ENST00000378842.8:c.875C>G
MANE Select
|
ENSP00000368119.4:p.Thr292Arg
|
|
ENST00000378842.7:c.875C>G
|
ENSP00000368119.3:p.Thr292Arg
|
|
ENST00000450095.6:c.548C>G
|
ENSP00000401956.2:p.Thr183Arg
|
|
ENST00000488412.2:n.131C>G
|
|
|
ENST00000489643.6:n.955C>G
|
|
|
ENST00000554550.5:c.*495C>G
|
ENSP00000451435.1:n.*495C>G
|
|
ENST00000554638.5:n.1347C>G
|
|
|
ENST00000555020.5:n.1336C>G
|
|
|
ENST00000555086.5:n.982C>G
|
|
|
ENST00000555754.1:n.323C>G
|
|
|
ENST00000556278.1:c.432+596C>G
|
ENSP00000451792.1:n.432+596C>G
|
|
ENST00000557706.5:n.1450C>G
|
|
|
NM_000155.3:c.875C>G
|
NP_000146.2:p.Thr292Arg
|
|
NM_001258332.1:c.548C>G
|
NP_001245261.1:p.Thr183Arg
|
|
NM_000155.4:c.875C>G
MANE Select
|
NP_000146.2:p.Thr292Arg
|
|
NM_001258332.2:c.548C>G
|
NP_001245261.1:p.Thr183Arg
|
|