ENST00000257863.9:c.1199A>T
MANE Select
|
ENSP00000257863.3:p.Asp400Val
|
|
ENST00000257863.8:c.1199A>T
|
ENSP00000257863.3:p.Asp400Val
|
|
ENST00000379791.7:c.1140+264A>T
|
ENSP00000369117.3:n.1140+264A>T
|
|
ENST00000550311.5:c.1199A>T
|
ENSP00000446661.1:p.Asp400Val
|
|
ENST00000550839.1:c.290A>T
|
ENSP00000455338.1:p.Asp97Val
|
|
ENST00000552233.5:n.787A>T
|
|
|
NM_001164690.1:c.1199A>T
|
NP_001158162.1:p.Asp400Val
|
|
NM_001164691.1:c.1140+264A>T
|
NP_001158163.1:n.1140+264A>T
|
|
NM_020547.2:c.1199A>T
|
NP_065434.1:p.Asp400Val
|
|
XM_011538173.1:c.1259A>T
|
XP_011536475.1:p.Asp420Val
|
|
XM_011538174.1:c.1256A>T
|
XP_011536476.1:p.Asp419Val
|
|
XM_011538175.1:c.1241A>T
|
XP_011536477.1:p.Asp414Val
|
|
XM_011538176.1:c.1202A>T
|
XP_011536478.1:p.Asp401Val
|
|
XM_011538177.1:c.1181A>T
|
XP_011536479.1:p.Asp394Val
|
|
XM_011538178.1:c.1040A>T
|
XP_011536480.1:p.Asp347Val
|
|
XM_011538179.1:c.1200+264A>T
|
XP_011536481.1:n.1200+264A>T
|
|
XM_011538180.1:c.926A>T
|
XP_011536482.1:p.Asp309Val
|
|
XM_011538181.1:c.923A>T
|
XP_011536483.1:p.Asp308Val
|
|
XM_011538182.1:c.848A>T
|
XP_011536484.1:p.Asp283Val
|
|
XM_011538183.1:c.1201-257A>T
|
XP_011536485.1:n.1201-257A>T
|
|
XM_011538184.1:c.1220+244A>T
|
XP_011536486.1:n.1220+244A>T
|
|
XM_011538185.1:c.856-1288A>T
|
XP_011536487.1:n.856-1288A>T
|
|
XM_011538186.1:c.374A>T
|
XP_011536488.1:p.Asp125Val
|
|
NM_001164690.2:c.1199A>T
|
NP_001158162.1:p.Asp400Val
|
|
NM_001164691.2:c.1140+264A>T
|
NP_001158163.1:n.1140+264A>T
|
|
NM_020547.3:c.1199A>T
MANE Select
|
NP_065434.1:p.Asp400Val
|
|
XM_011538183.2:c.1201-257A>T
|
XP_011536485.1:n.1201-257A>T
|
|
XM_011538184.2:c.1220+244A>T
|
XP_011536486.1:n.1220+244A>T
|
|
XM_011538186.3:c.374A>T
|
XP_011536488.1:p.Asp125Val
|
|
XM_017019179.2:c.1259A>T
|
XP_016874668.1:p.Asp420Val
|
|
XM_024448938.1:c.1143+264A>T
|
XP_024304706.1:n.1143+264A>T
|
|
XR_002957309.1:n.1167A>T
|
|
|
XR_002957310.1:n.1109-257A>T
|
|
|
XR_002957311.1:n.1167A>T
|
|
|
XR_002957312.1:n.1108+264A>T
|
|
|