|
NM_000154.2:c.447G>A
MANE Select
|
NP_000145.1:p.Thr149=
|
|
ENST00000588479.6:c.447G>A
MANE Select
|
ENSP00000465930.1:p.Thr149=
|
|
NM_000154.1:c.447G>A
|
NP_000145.1:p.Thr149=
|
|
NM_001381985.1:c.447G>A
|
NP_001368914.1:p.Thr149=
|
|
ENST00000225614.6:c.447G>A
|
ENSP00000225614.1:p.Thr149=
|
|
ENST00000586244.1:c.*171G>A
|
ENSP00000468288.1:n.*171G>A
|
|
ENST00000587707.1:c.201G>A
|
ENSP00000468341.1:p.Thr67=
|
|
ENST00000587707.2:c.447G>A
|
ENSP00000468341.2:p.Thr149=
|
|
ENST00000588479.5:c.447G>A
|
ENSP00000465930.1:p.Thr149=
|
|
ENST00000592494.1:n.468G>A
|
|
|
ENST00000592997.6:c.447G>A
|
ENSP00000464765.2:p.Thr149=
|