|
NM_014464.4:c.472T=
MANE Select
|
NP_055279.3:p.Ser158=
|
|
ENST00000259782.9:c.472T=
MANE Select
|
ENSP00000259782.4:p.Ser158=
|
|
NM_014464.3:c.472T=
|
NP_055279.3:p.Ser158=
|
|
ENST00000259782.8:c.472T=
|
ENSP00000259782.4:p.Ser158=
|
|
ENST00000370864.3:c.418T=
|
ENSP00000359901.3:p.Ser140=
|
|
ENST00000370869.7:c.460T=
|
ENSP00000359906.3:p.Ser154=
|
|
ENST00000486436.1:n.534T=
|
|
|
XM_006715061.2:c.481T=
|
XP_006715124.1:p.Ser161=
|
|
XM_006715062.2:c.418T=
|
XP_006715125.1:p.Ser140=
|
|
XM_006715063.2:c.481T=
|
XP_006715126.1:p.Ser161=
|
|
XM_011514496.1:c.365-5449T=
|
XP_011512798.1:n.365-5449T=
|
|
XM_011514497.1:c.356-5449T=
|
XP_011512799.1:n.356-5449T=
|
|
XM_011514497.2:c.356-5449T=
|
XP_011512799.1:n.356-5449T=
|
|
XM_011514498.1:c.256T=
|
XP_011512800.1:p.Ser86=
|
|
XM_011514499.1:c.140-5449T=
|
XP_011512801.1:n.140-5449T=
|
|
XM_017010745.1:c.472T=
|
XP_016866234.1:p.Ser158=
|
|
XM_017010746.1:c.247T=
|
XP_016866235.1:p.Ser83=
|
|
XM_017010747.1:c.131-5449T=
|
XP_016866236.1:n.131-5449T=
|
|
XM_017010748.1:c.-34T=
|
XP_016866237.1:n.-34T=
|
|
XR_001743344.2:n.582T=
|
|
|
XR_427828.2:n.514T=
|
|
