|
ENST00000478989.7:c.*214C>G
|
ENSP00000420645.3:n.*214C>G
|
|
|
ENST00000652321.2:c.1475C>G
|
ENSP00000498886.2:p.Thr492Arg
|
|
|
ENST00000287878.9:c.1478C>G
MANE Select
|
ENSP00000287878.3:p.Thr493Arg
|
|
|
ENST00000476632.2:c.755C>G
|
ENSP00000419493.2:p.Thr252Arg
|
|
|
ENST00000492843.6:c.1103C>G
|
ENSP00000419577.2:p.Thr368Arg
|
|
|
ENST00000650851.1:n.972C>G
|
|
|
|
ENST00000650858.1:c.695C>G
|
ENSP00000498384.1:p.Thr232Arg
|
|
|
ENST00000650948.1:n.3864C>G
|
|
|
|
ENST00000651188.1:c.*591C>G
|
ENSP00000498557.1:n.*591C>G
|
|
|
ENST00000651303.1:c.*797C>G
|
ENSP00000498428.1:n.*797C>G
|
|
|
ENST00000651378.1:c.755C>G
|
ENSP00000499103.1:p.Thr252Arg
|
|
|
ENST00000651764.1:c.1346C>G
|
ENSP00000498796.1:p.Thr449Arg
|
|
|
ENST00000651836.1:c.1668C>G
|
ENSP00000499156.1:n.1668C>G
|
|
|
ENST00000651954.1:n.1694C>G
|
|
|
|
ENST00000652047.1:c.1343C>G
|
ENSP00000499111.1:p.Thr448Arg
|
|
|
ENST00000652136.1:n.2025C>G
|
|
|
|
ENST00000652159.1:c.1346C>G
|
ENSP00000499025.1:p.Thr449Arg
|
|
|
ENST00000652397.1:c.*214C>G
|
ENSP00000498351.1:n.*214C>G
|
|
|
ENST00000287878.8:c.1478C>G
|
ENSP00000287878.3:p.Thr493Arg
|
|
|
ENST00000392801.6:c.1346C>G
|
ENSP00000376549.2:p.Thr449Arg
|
|
|
ENST00000418337.6:c.755C>G
|
ENSP00000387386.2:p.Thr252Arg
|
|
|
ENST00000479461.1:n.130C>G
|
|
|
|
ENST00000485183.1:n.131C>G
|
|
|
|
ENST00000492843.5:c.1106C>G
|
ENSP00000419577.1:p.Thr369Arg
|
|
|
NM_001040633.1:c.1346C>G
|
NP_001035723.1:p.Thr449Arg
|
|
|
NM_001304527.1:c.1103C>G
|
NP_001291456.1:p.Thr368Arg
|
|
|
NM_001304531.1:c.755C>G
|
NP_001291460.1:p.Thr252Arg
|
|
|
NM_016203.3:c.1478C>G
|
NP_057287.2:p.Thr493Arg
|
|
|
NM_024429.1:c.755C>G
|
NP_077747.1:p.Thr252Arg
|
|
|
XM_005250002.2:c.1478C>G
|
XP_005250059.1:p.Thr493Arg
|
|
|
XM_005250004.2:c.1346C>G
|
XP_005250061.1:p.Thr449Arg
|
|
|
XM_005250006.3:c.1106C>G
|
XP_005250063.1:p.Thr369Arg
|
|
|
XM_006716021.2:c.1466C>G
|
XP_006716084.1:p.Thr489Arg
|
|
|
XM_011516282.1:c.1463C>G
|
XP_011514584.1:p.Thr488Arg
|
|
|
XM_011516283.1:c.1466C>G
|
XP_011514585.1:p.Thr489Arg
|
|
|
XM_011516284.1:c.1463C>G
|
XP_011514586.1:p.Thr488Arg
|
|
|
XM_011516285.1:c.755C>G
|
XP_011514587.1:p.Thr252Arg
|
|
|
XM_011516286.1:c.731C>G
|
XP_011514588.1:p.Thr244Arg
|
|
|
XM_011516287.1:c.695C>G
|
XP_011514589.1:p.Thr232Arg
|
|
|
NM_001363698.1:c.1106C>G
|
NP_001350627.1:p.Thr369Arg
|
|
|
XM_005250002.4:c.1478C>G
|
XP_005250059.1:p.Thr493Arg
|
|
|
XM_005250004.4:c.1346C>G
|
XP_005250061.1:p.Thr449Arg
|
|
|
XM_005250006.5:c.1106C>G
|
XP_005250063.1:p.Thr369Arg
|
|
|
XM_011516285.2:c.755C>G
|
XP_011514587.1:p.Thr252Arg
|
|
|
XM_011516286.2:c.731C>G
|
XP_011514588.1:p.Thr244Arg
|
|
|
XM_017012268.2:c.1343C>G
|
XP_016867757.1:p.Thr448Arg
|
|
|
XM_017012269.1:c.1475C>G
|
XP_016867758.1:p.Thr492Arg
|
|
|
XM_017012270.1:c.1346C>G
|
XP_016867759.1:p.Thr449Arg
|
|
|
XM_017012271.2:c.1343C>G
|
XP_016867760.1:p.Thr448Arg
|
|
|
XM_017012272.1:c.1343C>G
|
XP_016867761.1:p.Thr448Arg
|
|
|
XM_017012274.2:c.752C>G
|
XP_016867763.1:p.Thr251Arg
|
|
|
XM_017012275.2:c.695C>G
|
XP_016867764.1:p.Thr232Arg
|
|
|
XM_017012276.2:c.752C>G
|
XP_016867765.1:p.Thr251Arg
|
|
|
XM_017012277.2:c.731C>G
|
XP_016867766.1:p.Thr244Arg
|
|
|
XM_017012278.1:c.695C>G
|
XP_016867767.1:p.Thr232Arg
|
|
|
XM_017012279.2:c.695C>G
|
XP_016867768.1:p.Thr232Arg
|
|
|
XM_017012280.2:c.695C>G
|
XP_016867769.1:p.Thr232Arg
|
|
|
XM_017012281.2:c.695C>G
|
XP_016867770.1:p.Thr232Arg
|
|
|
XM_024446786.1:c.1346C>G
|
XP_024302554.1:p.Thr449Arg
|
|
|
XM_024446787.1:c.755C>G
|
XP_024302555.1:p.Thr252Arg
|
|
|
XM_024446788.1:c.752C>G
|
XP_024302556.1:p.Thr251Arg
|
|
|
XM_024446789.1:c.755C>G
|
XP_024302557.1:p.Thr252Arg
|
|
|
NM_016203.4:c.1478C>G
MANE Select
|
NP_057287.2:p.Thr493Arg
|
|
|
NM_001040633.2:c.1346C>G
|
NP_001035723.1:p.Thr449Arg
|
|
|
NM_001304527.2:c.1103C>G
|
NP_001291456.1:p.Thr368Arg
|
|
|
NM_001304531.2:c.755C>G
|
NP_001291460.1:p.Thr252Arg
|
|
|
NM_001363698.2:c.1106C>G
|
NP_001350627.1:p.Thr369Arg
|
|
|
NM_024429.2:c.755C>G
|
NP_077747.1:p.Thr252Arg
|
|
