ENST00000257863.9:c.1155G>C
MANE Select
|
ENSP00000257863.3:p.Arg385Ser
|
|
ENST00000257863.8:c.1155G>C
|
ENSP00000257863.3:p.Arg385Ser
|
|
ENST00000379791.7:c.1140+220G>C
|
ENSP00000369117.3:n.1140+220G>C
|
|
ENST00000550311.5:c.1155G>C
|
ENSP00000446661.1:p.Arg385Ser
|
|
ENST00000550839.1:c.246G>C
|
ENSP00000455338.1:p.Arg82Ser
|
|
ENST00000552233.5:n.743G>C
|
|
|
NM_001164690.1:c.1155G>C
|
NP_001158162.1:p.Arg385Ser
|
|
NM_001164691.1:c.1140+220G>C
|
NP_001158163.1:n.1140+220G>C
|
|
NM_020547.2:c.1155G>C
|
NP_065434.1:p.Arg385Ser
|
|
XM_011538173.1:c.1215G>C
|
XP_011536475.1:p.Arg405Ser
|
|
XM_011538174.1:c.1212G>C
|
XP_011536476.1:p.Arg404Ser
|
|
XM_011538175.1:c.1197G>C
|
XP_011536477.1:p.Arg399Ser
|
|
XM_011538176.1:c.1158G>C
|
XP_011536478.1:p.Arg386Ser
|
|
XM_011538177.1:c.1137G>C
|
XP_011536479.1:p.Arg379Ser
|
|
XM_011538178.1:c.996G>C
|
XP_011536480.1:p.Arg332Ser
|
|
XM_011538179.1:c.1200+220G>C
|
XP_011536481.1:n.1200+220G>C
|
|
XM_011538180.1:c.882G>C
|
XP_011536482.1:p.Arg294Ser
|
|
XM_011538181.1:c.879G>C
|
XP_011536483.1:p.Arg293Ser
|
|
XM_011538182.1:c.804G>C
|
XP_011536484.1:p.Arg268Ser
|
|
XM_011538183.1:c.1200+220G>C
|
XP_011536485.1:n.1200+220G>C
|
|
XM_011538184.1:c.1220+200G>C
|
XP_011536486.1:n.1220+200G>C
|
|
XM_011538185.1:c.856-1332G>C
|
XP_011536487.1:n.856-1332G>C
|
|
XM_011538186.1:c.330G>C
|
XP_011536488.1:p.Arg110Ser
|
|
NM_001164690.2:c.1155G>C
|
NP_001158162.1:p.Arg385Ser
|
|
NM_001164691.2:c.1140+220G>C
|
NP_001158163.1:n.1140+220G>C
|
|
NM_020547.3:c.1155G>C
MANE Select
|
NP_065434.1:p.Arg385Ser
|
|
XM_011538183.2:c.1200+220G>C
|
XP_011536485.1:n.1200+220G>C
|
|
XM_011538184.2:c.1220+200G>C
|
XP_011536486.1:n.1220+200G>C
|
|
XM_011538186.3:c.330G>C
|
XP_011536488.1:p.Arg110Ser
|
|
XM_017019179.2:c.1215G>C
|
XP_016874668.1:p.Arg405Ser
|
|
XM_024448938.1:c.1143+220G>C
|
XP_024304706.1:n.1143+220G>C
|
|
XR_002957309.1:n.1123G>C
|
|
|
XR_002957310.1:n.1108+220G>C
|
|
|
XR_002957311.1:n.1123G>C
|
|
|
XR_002957312.1:n.1108+220G>C
|
|
|