ENST00000682565.1:c.7755T>G
|
ENSP00000507671.1:p.Thr2585=
|
|
ENST00000682801.1:c.7755T>G
|
ENSP00000507862.1:p.Thr2585=
|
|
ENST00000682859.1:c.7755T>G
|
ENSP00000508222.1:p.Thr2585=
|
|
ENST00000683791.1:c.1147T>G
|
|
|
ENST00000684460.1:c.5207T>G
|
|
|
ENST00000684548.1:c.7755T>G
|
ENSP00000507421.1:p.Thr2585=
|
|
ENST00000684590.1:c.2202T>G
|
ENSP00000507376.1:p.Thr734=
|
|
ENST00000684656.1:c.5207T>G
|
|
|
ENST00000613296.6:c.8136T>G
MANE Select
|
ENSP00000482968.1:p.Thr2712=
|
|
ENST00000651434.1:c.896-29680T>G
|
|
|
ENST00000423048.5:c.2967T>G
|
ENSP00000399833.1:p.Thr989=
|
|
ENST00000484298.5:c.8010T>G
|
ENSP00000478155.1:p.Thr2670=
|
|
ENST00000613296.4:c.8136T>G
|
ENSP00000482968.1:p.Thr2712=
|
|
ENST00000614410.4:c.8136T>G
|
ENSP00000479094.1:p.Thr2712=
|
|
ENST00000620466.4:n.1939T>G
|
|
|
NM_015120.4:c.8139T>G , LRG_741t1:c.8139T>G
|
NP_055935.4:p.Thr2713=
|
|
NM_001378454.1:c.8136T>G
MANE Select
|
NP_001365383.1:p.Thr2712=
|
|