ENST00000358755.5:c.1531C>T
MANE Select
|
ENSP00000351605.4:p.Arg511Cys
|
|
ENST00000358755.4:c.1531C>T
|
ENSP00000351605.4:p.Arg511Cys
|
|
ENST00000519011.5:c.*578C>T
|
ENSP00000427733.1:n.*578C>T
|
|
ENST00000521195.1:c.*1466C>T
|
ENSP00000428188.1:n.*1466C>T
|
|
ENST00000522484.5:c.1393-1249C>T
|
ENSP00000428301.1:n.1393-1249C>T
|
|
ENST00000522566.5:c.1531C>T
|
ENSP00000429055.1:p.Arg511Cys
|
|
ENST00000523739.5:c.1435C>T
|
ENSP00000429528.1:p.Arg479Cys
|
|
ENST00000523933.5:c.*578C>T
|
ENSP00000428257.1:n.*578C>T
|
|
NM_001164615.1:c.1531C>T
|
NP_001158087.1:p.Arg511Cys
|
|
NM_001164616.1:c.1435C>T
|
NP_001158088.1:p.Arg479Cys
|
|
NM_003506.3:c.1531C>T
|
NP_003497.2:p.Arg511Cys
|
|
XR_428385.2:n.1643-1249C>T
|
|
|
NM_001317796.1:c.616C>T
|
NP_001304725.1:p.Arg206Cys
|
|
NR_133921.1:n.1710-1249C>T
|
|
|
NM_003506.4:c.1531C>T
MANE Select
|
NP_003497.2:p.Arg511Cys
|
|
NM_001164615.2:c.1531C>T
|
NP_001158087.1:p.Arg511Cys
|
|
NM_001164616.2:c.1435C>T
|
NP_001158088.1:p.Arg479Cys
|
|
NM_001317796.2:c.616C>T
|
NP_001304725.1:p.Arg206Cys
|
|
NR_133921.2:n.1710-1249C>T
|
|
|