|
NM_006129.5:c.2424C>T
MANE Select
|
NP_006120.1:p.Phe808=
|
|
ENST00000306385.10:c.2424C>T
MANE Select
|
ENSP00000305714.5:p.Phe808=
|
|
NM_006129.4:c.2424C>T
|
NP_006120.1:p.Phe808=
|
|
NR_033403.1:n.2727C>T
|
|
|
NR_033403.2:n.2495C>T
|
|
|
ENST00000306385.9:c.2424C>T
|
ENSP00000305714.5:p.Phe808=
|
|
ENST00000354870.5:c.*1681C>T
|
ENSP00000346941.5:n.*1681C>T
|
|
ENST00000520626.5:c.*2956C>T
|
ENSP00000430015.1:n.*2956C>T
|
|
ENST00000520626.6:c.*2956C>T
|
ENSP00000430015.2:n.*2956C>T
|
|
ENST00000520970.5:c.*788C>T
|
ENSP00000428332.1:n.*788C>T
|
|
ENST00000520982.5:c.*1891C>T
|
ENSP00000428798.1:n.*1891C>T
|
|
XR_001745579.2:n.3317C>T
|
|
|
XR_949458.1:n.2797C>T
|
|
|
XR_949458.2:n.2739C>T
|
|