ENST00000257863.9:c.1210G>T
MANE Select
|
ENSP00000257863.3:p.Ala404Ser
|
|
ENST00000257863.8:c.1210G>T
|
ENSP00000257863.3:p.Ala404Ser
|
|
ENST00000379791.7:c.1140+275G>T
|
ENSP00000369117.3:n.1140+275G>T
|
|
ENST00000550311.5:c.1210G>T
|
ENSP00000446661.1:p.Ala404Ser
|
|
ENST00000550839.1:c.301G>T
|
ENSP00000455338.1:p.Ala101Ser
|
|
ENST00000552233.5:n.798G>T
|
|
|
NM_001164690.1:c.1210G>T
|
NP_001158162.1:p.Ala404Ser
|
|
NM_001164691.1:c.1140+275G>T
|
NP_001158163.1:n.1140+275G>T
|
|
NM_020547.2:c.1210G>T
|
NP_065434.1:p.Ala404Ser
|
|
XM_011538173.1:c.1270G>T
|
XP_011536475.1:p.Ala424Ser
|
|
XM_011538174.1:c.1267G>T
|
XP_011536476.1:p.Ala423Ser
|
|
XM_011538175.1:c.1252G>T
|
XP_011536477.1:p.Ala418Ser
|
|
XM_011538176.1:c.1213G>T
|
XP_011536478.1:p.Ala405Ser
|
|
XM_011538177.1:c.1192G>T
|
XP_011536479.1:p.Ala398Ser
|
|
XM_011538178.1:c.1051G>T
|
XP_011536480.1:p.Ala351Ser
|
|
XM_011538179.1:c.1200+275G>T
|
XP_011536481.1:n.1200+275G>T
|
|
XM_011538180.1:c.937G>T
|
XP_011536482.1:p.Ala313Ser
|
|
XM_011538181.1:c.934G>T
|
XP_011536483.1:p.Ala312Ser
|
|
XM_011538182.1:c.859G>T
|
XP_011536484.1:p.Ala287Ser
|
|
XM_011538183.1:c.1201-246G>T
|
XP_011536485.1:n.1201-246G>T
|
|
XM_011538184.1:c.1220+255G>T
|
XP_011536486.1:n.1220+255G>T
|
|
XM_011538185.1:c.856-1277G>T
|
XP_011536487.1:n.856-1277G>T
|
|
XM_011538186.1:c.385G>T
|
XP_011536488.1:p.Ala129Ser
|
|
NM_001164690.2:c.1210G>T
|
NP_001158162.1:p.Ala404Ser
|
|
NM_001164691.2:c.1140+275G>T
|
NP_001158163.1:n.1140+275G>T
|
|
NM_020547.3:c.1210G>T
MANE Select
|
NP_065434.1:p.Ala404Ser
|
|
XM_011538183.2:c.1201-246G>T
|
XP_011536485.1:n.1201-246G>T
|
|
XM_011538184.2:c.1220+255G>T
|
XP_011536486.1:n.1220+255G>T
|
|
XM_011538186.3:c.385G>T
|
XP_011536488.1:p.Ala129Ser
|
|
XM_017019179.2:c.1270G>T
|
XP_016874668.1:p.Ala424Ser
|
|
XM_024448938.1:c.1143+275G>T
|
XP_024304706.1:n.1143+275G>T
|
|
XR_002957309.1:n.1178G>T
|
|
|
XR_002957310.1:n.1109-246G>T
|
|
|
XR_002957311.1:n.1178G>T
|
|
|
XR_002957312.1:n.1108+275G>T
|
|
|