|
ENST00000257863.9:c.1288+39_1288+43delinsCCCCG
MANE Select
|
ENSP00000257863.3:n.1288+39_1288+43delinsCCCCG
|
|
|
ENST00000257863.8:c.1288+39_1288+43delinsCCCCG
|
ENSP00000257863.3:n.1288+39_1288+43delinsCCCCG
|
|
|
ENST00000379791.7:c.1140+392_1140+396delinsCCCCG
|
ENSP00000369117.3:n.1140+392_1140+396delinsCCCCG
|
|
|
ENST00000550311.5:c.1288+39_1288+43delinsCCCCG
|
ENSP00000446661.1:n.1288+39_1288+43delinsCCCCG
|
|
|
ENST00000550839.1:c.379+39_379+43delinsCCCCG
|
ENSP00000455338.1:n.379+39_379+43delinsCCCCG
|
|
|
ENST00000552233.5:n.915_919delinsCCCCG
|
|
|
|
NM_001164690.1:c.1288+39_1288+43delinsCCCCG
|
NP_001158162.1:n.1288+39_1288+43delinsCCCCG
|
|
|
NM_001164691.1:c.1140+392_1140+396delinsCCCCG
|
NP_001158163.1:n.1140+392_1140+396delinsCCCCG
|
|
|
NM_020547.2:c.1288+39_1288+43delinsCCCCG
|
NP_065434.1:n.1288+39_1288+43delinsCCCCG
|
|
|
XM_011538173.1:c.1348+39_1348+43delinsCCCCG
|
XP_011536475.1:n.1348+39_1348+43delinsCCCCG
|
|
|
XM_011538174.1:c.1345+39_1345+43delinsCCCCG
|
XP_011536476.1:n.1345+39_1345+43delinsCCCCG
|
|
|
XM_011538175.1:c.1330+39_1330+43delinsCCCCG
|
XP_011536477.1:n.1330+39_1330+43delinsCCCCG
|
|
|
XM_011538176.1:c.1291+39_1291+43delinsCCCCG
|
XP_011536478.1:n.1291+39_1291+43delinsCCCCG
|
|
|
XM_011538177.1:c.1270+39_1270+43delinsCCCCG
|
XP_011536479.1:n.1270+39_1270+43delinsCCCCG
|
|
|
XM_011538178.1:c.1129+39_1129+43delinsCCCCG
|
XP_011536480.1:n.1129+39_1129+43delinsCCCCG
|
|
|
XM_011538179.1:c.1200+392_1200+396delinsCCCCG
|
XP_011536481.1:n.1200+392_1200+396delinsCCCCG
|
|
|
XM_011538180.1:c.1015+39_1015+43delinsCCCCG
|
XP_011536482.1:n.1015+39_1015+43delinsCCCCG
|
|
|
XM_011538181.1:c.1012+39_1012+43delinsCCCCG
|
XP_011536483.1:n.1012+39_1012+43delinsCCCCG
|
|
|
XM_011538182.1:c.937+39_937+43delinsCCCCG
|
XP_011536484.1:n.937+39_937+43delinsCCCCG
|
|
|
XM_011538183.1:c.1201-129_1201-125delinsCCCCG
|
XP_011536485.1:n.1201-129_1201-125delinsCCCCG
|
|
|
XM_011538184.1:c.1220+372_1220+376delinsCCCCG
|
XP_011536486.1:n.1220+372_1220+376delinsCCCCG
|
|
|
XM_011538185.1:c.856-1160_856-1156delinsCCCCG
|
XP_011536487.1:n.856-1160_856-1156delinsCCCCG
|
|
|
XM_011538186.1:c.463+39_463+43delinsCCCCG
|
XP_011536488.1:n.463+39_463+43delinsCCCCG
|
|
|
NM_001164690.2:c.1288+39_1288+43delinsCCCCG
|
NP_001158162.1:n.1288+39_1288+43delinsCCCCG
|
|
|
NM_001164691.2:c.1140+392_1140+396delinsCCCCG
|
NP_001158163.1:n.1140+392_1140+396delinsCCCCG
|
|
|
NM_020547.3:c.1288+39_1288+43delinsCCCCG
MANE Select
|
NP_065434.1:n.1288+39_1288+43delinsCCCCG
|
|
|
XM_011538183.2:c.1201-129_1201-125delinsCCCCG
|
XP_011536485.1:n.1201-129_1201-125delinsCCCCG
|
|
|
XM_011538184.2:c.1220+372_1220+376delinsCCCCG
|
XP_011536486.1:n.1220+372_1220+376delinsCCCCG
|
|
|
XM_011538186.3:c.463+39_463+43delinsCCCCG
|
XP_011536488.1:n.463+39_463+43delinsCCCCG
|
|
|
XM_017019179.2:c.1348+39_1348+43delinsCCCCG
|
XP_016874668.1:n.1348+39_1348+43delinsCCCCG
|
|
|
XM_024448938.1:c.1143+392_1143+396delinsCCCCG
|
XP_024304706.1:n.1143+392_1143+396delinsCCCCG
|
|
|
XR_002957309.1:n.1256+39_1256+43delinsCCCCG
|
|
|
|
XR_002957310.1:n.1109-129_1109-125delinsCCCCG
|
|
|
|
XR_002957311.1:n.1256+39_1256+43delinsCCCCG
|
|
|
|
XR_002957312.1:n.1108+392_1108+396delinsCCCCG
|
|
|
