ENST00000297598.5:c.1581T>G
MANE Select
|
ENSP00000297598.4:p.Ser527=
|
|
ENST00000297598.4:c.1581T>G
|
ENSP00000297598.4:p.Ser527=
|
|
ENST00000396200.3:c.1656T>G
|
ENSP00000379503.3:p.Ser552=
|
|
ENST00000517764.1:c.1581T>G
|
ENSP00000430380.1:p.Ser527=
|
|
ENST00000520728.5:c.1581T>G
|
ENSP00000428317.1:p.Ser527=
|
|
NM_001161779.1:c.1656T>G
|
NP_001155251.1:p.Ser552=
|
|
NM_001161780.1:c.1656T>G
|
NP_001155252.1:p.Ser552=
|
|
NM_001161781.1:c.1581T>G
|
NP_001155253.1:p.Ser527=
|
|
NM_018444.3:c.1581T>G
|
NP_060914.2:p.Ser527=
|
|
XM_011517135.1:c.1635T>G
|
XP_011515437.1:p.Ser545=
|
|
XM_011517136.1:c.1581T>G
|
XP_011515438.1:p.Ser527=
|
|
XM_011517137.1:c.1581T>G
|
XP_011515439.1:p.Ser527=
|
|
XM_011517135.2:c.1635T>G
|
XP_011515437.1:p.Ser545=
|
|
XM_011517136.2:c.1581T>G
|
XP_011515438.1:p.Ser527=
|
|
XM_017013588.1:c.1743T>G
|
XP_016869077.1:p.Ser581=
|
|
NM_018444.4:c.1581T>G
MANE Select
|
NP_060914.2:p.Ser527=
|
|
NM_001161780.2:c.1656T>G
|
NP_001155252.1:p.Ser552=
|
|
NM_001161781.2:c.1581T>G
|
NP_001155253.1:p.Ser527=
|
|
NM_001161779.2:c.1656T>G
|
NP_001155251.1:p.Ser552=
|
|