ENST00000263121.12:c.353C>G
|
ENSP00000263121.8:p.Thr118Ser
|
|
ENST00000344921.11:c.326C>G
|
ENSP00000340883.6:p.Thr109Ser
|
|
ENST00000407082.4:c.326C>G
|
ENSP00000385226.4:p.Thr109Ser
|
|
ENST00000407422.8:c.326C>G
|
ENSP00000383984.3:p.Thr109Ser
|
|
ENST00000417137.6:c.353C>G
|
ENSP00000388489.2:p.Thr118Ser
|
|
ENST00000491967.2:n.516C>G
|
|
|
ENST00000643421.1:n.321C>G
|
|
|
ENST00000644036.2:c.353C>G
MANE Select
|
ENSP00000494049.2:p.Thr118Ser
|
|
ENST00000644462.1:c.188C>G
|
ENSP00000494283.1:p.Thr63Ser
|
|
ENST00000644619.1:c.353C>G
|
ENSP00000494695.1:p.Thr118Ser
|
|
ENST00000646421.1:n.2209C>G
|
|
|
ENST00000646723.1:n.341C>G
|
|
|
ENST00000646911.1:n.265C>G
|
|
|
ENST00000647057.1:c.93+6417C>G
|
ENSP00000494757.1:n.93+6417C>G
|
|
ENST00000263121.11:c.353C>G
|
ENSP00000263121.7:p.Thr118Ser
|
|
ENST00000344921.10:c.326C>G
|
ENSP00000340883.6:p.Thr109Ser
|
|
ENST00000407082.3:c.353C>G
|
ENSP00000385226.3:p.Thr118Ser
|
|
ENST00000407422.7:c.326C>G
|
ENSP00000383984.3:p.Thr109Ser
|
|
ENST00000417137.5:c.353C>G
|
ENSP00000388489.1:p.Thr118Ser
|
|
ENST00000491967.1:n.79C>G
|
|
|
ENST00000634926.1:c.205C>G
|
|
|
ENST00000635578.1:c.178C>G
|
|
|
NM_001007468.1:c.326C>G
|
NP_001007469.1:p.Thr109Ser
|
|
NM_003073.3:c.353C>G , LRG_520t1:c.353C>G
|
NP_003064.2:p.Thr118Ser
|
|
XM_011530345.1:c.353C>G
|
XP_011528647.1:p.Thr118Ser
|
|
XM_011530346.1:c.326C>G
|
XP_011528648.1:p.Thr109Ser
|
|
NM_001007468.2:c.326C>G
|
NP_001007469.1:p.Thr109Ser
|
|
NM_001317946.1:c.326C>G
|
NP_001304875.1:p.Thr109Ser
|
|
NM_001362877.1:c.353C>G
|
NP_001349806.1:p.Thr118Ser
|
|
NM_003073.4:c.353C>G
|
NP_003064.2:p.Thr118Ser
|
|
NM_001007468.3:c.326C>G
|
NP_001007469.1:p.Thr109Ser
|
|
NM_001317946.2:c.326C>G
|
NP_001304875.1:p.Thr109Ser
|
|
NM_001362877.2:c.353C>G
|
NP_001349806.1:p.Thr118Ser
|
|
NM_003073.5:c.353C>G
MANE Select
|
NP_003064.2:p.Thr118Ser
|
|