ENST00000260947.9:c.1251G>T
MANE Select
|
ENSP00000260947.4:p.Leu417Phe
|
|
ENST00000421162.2:c.215+16438G>T
|
ENSP00000392245.2:n.215+16438G>T
|
|
ENST00000613192.2:c.158+28789G>T
|
ENSP00000483275.2:n.158+28789G>T
|
|
ENST00000613374.5:c.159-28068G>T
|
ENSP00000484464.1:n.159-28068G>T
|
|
ENST00000613706.5:c.906+345G>T
|
ENSP00000484976.2:n.906+345G>T
|
|
ENST00000617164.5:c.1194G>T
|
ENSP00000480470.1:p.Leu398Phe
|
|
ENST00000619009.5:c.364+11674G>T
|
ENSP00000482293.1:n.364+11674G>T
|
|
ENST00000650978.1:c.1093G>T
|
|
|
ENST00000260947.8:c.1251G>T
|
ENSP00000260947.4:p.Leu417Phe
|
|
ENST00000421162.1:c.215+16438G>T
|
ENSP00000392245.1:n.215+16438G>T
|
|
ENST00000455743.5:c.*871G>T
|
ENSP00000412186.1:n.*871G>T
|
|
ENST00000613192.1:c.73+28789G>T
|
ENSP00000483275.1:n.73+28789G>T
|
|
ENST00000613374.4:c.159-28068G>T
|
ENSP00000484464.1:n.159-28068G>T
|
|
ENST00000613706.4:c.215+16438G>T
|
ENSP00000484976.1:n.215+16438G>T
|
|
ENST00000617164.4:c.1194G>T
|
ENSP00000480470.1:p.Leu398Phe
|
|
ENST00000619009.4:c.364+11674G>T
|
ENSP00000482293.1:n.364+11674G>T
|
|
ENST00000620057.4:c.365-11311G>T
|
ENSP00000481988.1:n.365-11311G>T
|
|
NM_000465.3:c.1251G>T
|
NP_000456.2:p.Leu417Phe
|
|
NM_001282543.1:c.1194G>T
|
NP_001269472.1:p.Leu398Phe
|
|
NM_001282545.1:c.215+16438G>T
|
NP_001269474.1:n.215+16438G>T
|
|
NM_001282548.1:c.159-28068G>T
|
NP_001269477.1:n.159-28068G>T
|
|
NM_001282549.1:c.364+11674G>T
|
NP_001269478.1:n.364+11674G>T
|
|
NR_104212.1:n.1244G>T
|
|
|
NR_104215.1:n.1187G>T
|
|
|
NR_104216.1:n.507-11311G>T
|
|
|
XM_011511567.1:c.1197G>T
|
XP_011509869.1:p.Leu399Phe
|
|
XM_011511568.1:c.1251G>T
|
XP_011509870.1:p.Leu417Phe
|
|
XM_017004613.1:c.1350G>T
|
XP_016860102.1:p.Leu450Phe
|
|
XM_017004614.1:c.1350G>T
|
XP_016860103.1:p.Leu450Phe
|
|
XR_002959322.1:n.1441G>T
|
|
|
NM_000465.4:c.1251G>T
MANE Select
|
NP_000456.2:p.Leu417Phe
|
|
NM_001282543.2:c.1194G>T
|
NP_001269472.1:p.Leu398Phe
|
|
NM_001282545.2:c.215+16438G>T
|
NP_001269474.1:n.215+16438G>T
|
|
NM_001282548.2:c.159-28068G>T
|
NP_001269477.1:n.159-28068G>T
|
|
NM_001282549.2:c.364+11674G>T
|
NP_001269478.1:n.364+11674G>T
|
|
NR_104212.2:n.1216G>T
|
|
|
NR_104215.2:n.1159G>T
|
|
|
NR_104216.2:n.479-11311G>T
|
|
|