|
ENST00000260947.9:c.705T=
MANE Select
|
ENSP00000260947.4:p.Ser235=
|
|
|
ENST00000421162.2:c.215+15892T=
|
ENSP00000392245.2:n.215+15892T=
|
|
|
ENST00000613192.2:c.158+28243T=
|
ENSP00000483275.2:n.158+28243T=
|
|
|
ENST00000613374.5:c.158+28243T=
|
ENSP00000484464.1:n.158+28243T=
|
|
|
ENST00000613706.5:c.705T=
|
ENSP00000484976.2:p.Ser235=
|
|
|
ENST00000617164.5:c.648T=
|
ENSP00000480470.1:p.Ser216=
|
|
|
ENST00000619009.5:c.364+11128T=
|
ENSP00000482293.1:n.364+11128T=
|
|
|
ENST00000650978.1:c.547T=
|
|
|
|
ENST00000260947.8:c.705T=
|
ENSP00000260947.4:p.Ser235=
|
|
|
ENST00000421162.1:c.215+15892T=
|
ENSP00000392245.1:n.215+15892T=
|
|
|
ENST00000455743.5:c.*325T=
|
ENSP00000412186.1:n.*325T=
|
|
|
ENST00000471787.1:n.600T=
|
|
|
|
ENST00000613192.1:c.73+28243T=
|
ENSP00000483275.1:n.73+28243T=
|
|
|
ENST00000613374.4:c.158+28243T=
|
ENSP00000484464.1:n.158+28243T=
|
|
|
ENST00000613706.4:c.215+15892T=
|
ENSP00000484976.1:n.215+15892T=
|
|
|
ENST00000617164.4:c.648T=
|
ENSP00000480470.1:p.Ser216=
|
|
|
ENST00000619009.4:c.364+11128T=
|
ENSP00000482293.1:n.364+11128T=
|
|
|
ENST00000620057.4:c.364+11128T=
|
ENSP00000481988.1:n.364+11128T=
|
|
|
NM_000465.3:c.705T=
|
NP_000456.2:p.Ser235=
|
|
|
NM_001282543.1:c.648T=
|
NP_001269472.1:p.Ser216=
|
|
|
NM_001282545.1:c.215+15892T=
|
NP_001269474.1:n.215+15892T=
|
|
|
NM_001282548.1:c.158+28243T=
|
NP_001269477.1:n.158+28243T=
|
|
|
NM_001282549.1:c.364+11128T=
|
NP_001269478.1:n.364+11128T=
|
|
|
NR_104212.1:n.698T=
|
|
|
|
NR_104215.1:n.641T=
|
|
|
|
NR_104216.1:n.506+11128T=
|
|
|
|
XM_011511567.1:c.651T=
|
XP_011509869.1:p.Ser217=
|
|
|
XM_011511568.1:c.705T=
|
XP_011509870.1:p.Ser235=
|
|
|
XM_017004613.1:c.804T=
|
XP_016860102.1:p.Ser268=
|
|
|
XM_017004614.1:c.804T=
|
XP_016860103.1:p.Ser268=
|
|
|
XR_002959322.1:n.895T=
|
|
|
|
NM_000465.4:c.705T=
MANE Select
|
NP_000456.2:p.Ser235=
|
|
|
NM_001282543.2:c.648T=
|
NP_001269472.1:p.Ser216=
|
|
|
NM_001282545.2:c.215+15892T=
|
NP_001269474.1:n.215+15892T=
|
|
|
NM_001282548.2:c.158+28243T=
|
NP_001269477.1:n.158+28243T=
|
|
|
NM_001282549.2:c.364+11128T=
|
NP_001269478.1:n.364+11128T=
|
|
|
NR_104212.2:n.670T=
|
|
|
|
NR_104215.2:n.613T=
|
|
|
|
NR_104216.2:n.478+11128T=
|
|
|
