ENST00000297598.5:c.1457C=
MANE Select
|
ENSP00000297598.4:p.Ala486=
|
|
ENST00000297598.4:c.1457C=
|
ENSP00000297598.4:p.Ala486=
|
|
ENST00000396200.3:c.1532C=
|
ENSP00000379503.3:p.Ala511=
|
|
ENST00000517764.1:c.1457C=
|
ENSP00000430380.1:p.Ala486=
|
|
ENST00000520728.5:c.1457C=
|
ENSP00000428317.1:p.Ala486=
|
|
NM_001161779.1:c.1532C=
|
NP_001155251.1:p.Ala511=
|
|
NM_001161780.1:c.1532C=
|
NP_001155252.1:p.Ala511=
|
|
NM_001161781.1:c.1457C=
|
NP_001155253.1:p.Ala486=
|
|
NM_018444.3:c.1457C=
|
NP_060914.2:p.Ala486=
|
|
XM_011517135.1:c.1511C=
|
XP_011515437.1:p.Ala504=
|
|
XM_011517136.1:c.1457C=
|
XP_011515438.1:p.Ala486=
|
|
XM_011517137.1:c.1457C=
|
XP_011515439.1:p.Ala486=
|
|
XM_011517135.2:c.1511C=
|
XP_011515437.1:p.Ala504=
|
|
XM_011517136.2:c.1457C=
|
XP_011515438.1:p.Ala486=
|
|
XM_017013588.1:c.1619C=
|
XP_016869077.1:p.Ala540=
|
|
NM_018444.4:c.1457C=
MANE Select
|
NP_060914.2:p.Ala486=
|
|
NM_001161780.2:c.1532C=
|
NP_001155252.1:p.Ala511=
|
|
NM_001161781.2:c.1457C=
|
NP_001155253.1:p.Ala486=
|
|
NM_001161779.2:c.1532C=
|
NP_001155251.1:p.Ala511=
|
|