ENST00000682565.1:c.10094G>C
|
ENSP00000507671.1:p.Ser3365Thr
|
|
ENST00000682801.1:c.10094G>C
|
ENSP00000507862.1:p.Ser3365Thr
|
|
ENST00000682859.1:c.10094G>C
|
ENSP00000508222.1:p.Ser3365Thr
|
|
ENST00000683791.1:c.3180G>C
|
|
|
ENST00000684460.1:c.7375G>C
|
|
|
ENST00000684548.1:c.10094G>C
|
ENSP00000507421.1:p.Ser3365Thr
|
|
ENST00000684590.1:c.4541G>C
|
ENSP00000507376.1:p.Ser1514Thr
|
|
ENST00000684656.1:c.7420G>C
|
|
|
ENST00000613296.6:c.10475G>C
MANE Select
|
ENSP00000482968.1:p.Ser3492Thr
|
|
ENST00000651057.1:c.629G>C
|
ENSP00000498504.1:p.Ser210Thr
|
|
ENST00000651434.1:c.1831G>C
|
|
|
ENST00000652487.1:c.1572G>C
|
|
|
ENST00000423048.5:c.3966G>C
|
ENSP00000399833.1:n.3966G>C
|
|
ENST00000484298.5:c.10349G>C
|
ENSP00000478155.1:p.Ser3450Thr
|
|
ENST00000613296.4:c.10475G>C
|
ENSP00000482968.1:p.Ser3492Thr
|
|
ENST00000614410.4:c.10475G>C
|
ENSP00000479094.1:p.Ser3492Thr
|
|
ENST00000620466.4:n.4278G>C
|
|
|
NM_015120.4:c.10478G>C , LRG_741t1:c.10478G>C
|
NP_055935.4:p.Ser3493Thr
|
|
NM_001378454.1:c.10475G>C
MANE Select
|
NP_001365383.1:p.Ser3492Thr
|
|