ENST00000508051.2:c.829C>T
|
ENSP00000513677.1:p.Pro277Ser
|
|
ENST00000698351.1:c.864+796C>T
|
ENSP00000513674.1:n.864+796C>T
|
|
ENST00000698352.1:c.*1212C>T
|
ENSP00000513675.1:n.*1212C>T
|
|
ENST00000698353.1:n.1535C>T
|
|
|
ENST00000698354.1:c.829C>T
|
ENSP00000513676.1:p.Pro277Ser
|
|
ENST00000296795.8:c.1660C>T
MANE Select
|
ENSP00000296795.3:p.Pro554Ser
|
|
ENST00000296795.7:c.1660C>T
|
ENSP00000296795.2:p.Pro554Ser
|
|
ENST00000504367.1:c.829C>T
|
ENSP00000423684.1:p.Pro277Ser
|
|
ENST00000512264.1:n.1736C>T
|
|
|
NM_003265.2:c.1660C>T , LRG_117t1:c.1660C>T
|
NP_003256.1:p.Pro554Ser
|
|
NM_003265.3:c.1660C>T
MANE Select
|
NP_003256.1:p.Pro554Ser
|
|