ENST00000257863.9:c.1147A>T
MANE Select
|
ENSP00000257863.3:p.Thr383Ser
|
|
ENST00000257863.8:c.1147A>T
|
ENSP00000257863.3:p.Thr383Ser
|
|
ENST00000379791.7:c.1140+212A>T
|
ENSP00000369117.3:n.1140+212A>T
|
|
ENST00000550311.5:c.1147A>T
|
ENSP00000446661.1:p.Thr383Ser
|
|
ENST00000550839.1:c.238A>T
|
ENSP00000455338.1:p.Thr80Ser
|
|
ENST00000552233.5:n.735A>T
|
|
|
NM_001164690.1:c.1147A>T
|
NP_001158162.1:p.Thr383Ser
|
|
NM_001164691.1:c.1140+212A>T
|
NP_001158163.1:n.1140+212A>T
|
|
NM_020547.2:c.1147A>T
|
NP_065434.1:p.Thr383Ser
|
|
XM_011538173.1:c.1207A>T
|
XP_011536475.1:p.Thr403Ser
|
|
XM_011538174.1:c.1204A>T
|
XP_011536476.1:p.Thr402Ser
|
|
XM_011538175.1:c.1189A>T
|
XP_011536477.1:p.Thr397Ser
|
|
XM_011538176.1:c.1150A>T
|
XP_011536478.1:p.Thr384Ser
|
|
XM_011538177.1:c.1129A>T
|
XP_011536479.1:p.Thr377Ser
|
|
XM_011538178.1:c.988A>T
|
XP_011536480.1:p.Thr330Ser
|
|
XM_011538179.1:c.1200+212A>T
|
XP_011536481.1:n.1200+212A>T
|
|
XM_011538180.1:c.874A>T
|
XP_011536482.1:p.Thr292Ser
|
|
XM_011538181.1:c.871A>T
|
XP_011536483.1:p.Thr291Ser
|
|
XM_011538182.1:c.796A>T
|
XP_011536484.1:p.Thr266Ser
|
|
XM_011538183.1:c.1200+212A>T
|
XP_011536485.1:n.1200+212A>T
|
|
XM_011538184.1:c.1220+192A>T
|
XP_011536486.1:n.1220+192A>T
|
|
XM_011538185.1:c.856-1340A>T
|
XP_011536487.1:n.856-1340A>T
|
|
XM_011538186.1:c.322A>T
|
XP_011536488.1:p.Thr108Ser
|
|
NM_001164690.2:c.1147A>T
|
NP_001158162.1:p.Thr383Ser
|
|
NM_001164691.2:c.1140+212A>T
|
NP_001158163.1:n.1140+212A>T
|
|
NM_020547.3:c.1147A>T
MANE Select
|
NP_065434.1:p.Thr383Ser
|
|
XM_011538183.2:c.1200+212A>T
|
XP_011536485.1:n.1200+212A>T
|
|
XM_011538184.2:c.1220+192A>T
|
XP_011536486.1:n.1220+192A>T
|
|
XM_011538186.3:c.322A>T
|
XP_011536488.1:p.Thr108Ser
|
|
XM_017019179.2:c.1207A>T
|
XP_016874668.1:p.Thr403Ser
|
|
XM_024448938.1:c.1143+212A>T
|
XP_024304706.1:n.1143+212A>T
|
|
XR_002957309.1:n.1115A>T
|
|
|
XR_002957310.1:n.1108+212A>T
|
|
|
XR_002957311.1:n.1115A>T
|
|
|
XR_002957312.1:n.1108+212A>T
|
|
|