ENST00000682565.1:c.7392T>C
|
ENSP00000507671.1:p.Thr2464=
|
|
ENST00000682801.1:c.7392T>C
|
ENSP00000507862.1:p.Thr2464=
|
|
ENST00000682859.1:c.7392T>C
|
ENSP00000508222.1:p.Thr2464=
|
|
ENST00000683791.1:c.784T>C
|
|
|
ENST00000684460.1:c.4844T>C
|
|
|
ENST00000684548.1:c.7392T>C
|
ENSP00000507421.1:p.Thr2464=
|
|
ENST00000684590.1:c.1839T>C
|
ENSP00000507376.1:p.Thr613=
|
|
ENST00000684656.1:c.4844T>C
|
|
|
ENST00000613296.6:c.7773T>C
MANE Select
|
ENSP00000482968.1:p.Thr2591=
|
|
ENST00000651434.1:c.896-30043T>C
|
|
|
ENST00000423048.5:c.2604T>C
|
ENSP00000399833.1:p.Thr868=
|
|
ENST00000484298.5:c.7647T>C
|
ENSP00000478155.1:p.Thr2549=
|
|
ENST00000613296.4:c.7773T>C
|
ENSP00000482968.1:p.Thr2591=
|
|
ENST00000614410.4:c.7773T>C
|
ENSP00000479094.1:p.Thr2591=
|
|
ENST00000620466.4:n.1576T>C
|
|
|
NM_015120.4:c.7776T>C , LRG_741t1:c.7776T>C
|
NP_055935.4:p.Thr2592=
|
|
NM_001378454.1:c.7773T>C
MANE Select
|
NP_001365383.1:p.Thr2591=
|
|