|
NM_006129.5:c.2487C>T
MANE Select
|
NP_006120.1:p.Pro829=
|
|
ENST00000306385.10:c.2487C>T
MANE Select
|
ENSP00000305714.5:p.Pro829=
|
|
NM_006129.4:c.2487C>T
|
NP_006120.1:p.Pro829=
|
|
NR_033403.1:n.2790C>T
|
|
|
NR_033403.2:n.2558C>T
|
|
|
ENST00000306385.9:c.2487C>T
|
ENSP00000305714.5:p.Pro829=
|
|
ENST00000354870.5:c.*1744C>T
|
ENSP00000346941.5:n.*1744C>T
|
|
ENST00000520626.5:c.*3019C>T
|
ENSP00000430015.1:n.*3019C>T
|
|
ENST00000520626.6:c.*3019C>T
|
ENSP00000430015.2:n.*3019C>T
|
|
ENST00000520970.5:c.*851C>T
|
ENSP00000428332.1:n.*851C>T
|
|
ENST00000520982.5:c.*1954C>T
|
ENSP00000428798.1:n.*1954C>T
|
|
XR_001745579.2:n.3380C>T
|
|
|
XR_949458.1:n.2860C>T
|
|
|
XR_949458.2:n.2802C>T
|
|