ENST00000257863.9:c.1232A>C
MANE Select
|
ENSP00000257863.3:p.Tyr411Ser
|
|
ENST00000257863.8:c.1232A>C
|
ENSP00000257863.3:p.Tyr411Ser
|
|
ENST00000379791.7:c.1140+297A>C
|
ENSP00000369117.3:n.1140+297A>C
|
|
ENST00000550311.5:c.1232A>C
|
ENSP00000446661.1:p.Tyr411Ser
|
|
ENST00000550839.1:c.323A>C
|
ENSP00000455338.1:p.Tyr108Ser
|
|
ENST00000552233.5:n.820A>C
|
|
|
NM_001164690.1:c.1232A>C
|
NP_001158162.1:p.Tyr411Ser
|
|
NM_001164691.1:c.1140+297A>C
|
NP_001158163.1:n.1140+297A>C
|
|
NM_020547.2:c.1232A>C
|
NP_065434.1:p.Tyr411Ser
|
|
XM_011538173.1:c.1292A>C
|
XP_011536475.1:p.Tyr431Ser
|
|
XM_011538174.1:c.1289A>C
|
XP_011536476.1:p.Tyr430Ser
|
|
XM_011538175.1:c.1274A>C
|
XP_011536477.1:p.Tyr425Ser
|
|
XM_011538176.1:c.1235A>C
|
XP_011536478.1:p.Tyr412Ser
|
|
XM_011538177.1:c.1214A>C
|
XP_011536479.1:p.Tyr405Ser
|
|
XM_011538178.1:c.1073A>C
|
XP_011536480.1:p.Tyr358Ser
|
|
XM_011538179.1:c.1200+297A>C
|
XP_011536481.1:n.1200+297A>C
|
|
XM_011538180.1:c.959A>C
|
XP_011536482.1:p.Tyr320Ser
|
|
XM_011538181.1:c.956A>C
|
XP_011536483.1:p.Tyr319Ser
|
|
XM_011538182.1:c.881A>C
|
XP_011536484.1:p.Tyr294Ser
|
|
XM_011538183.1:c.1201-224A>C
|
XP_011536485.1:n.1201-224A>C
|
|
XM_011538184.1:c.1220+277A>C
|
XP_011536486.1:n.1220+277A>C
|
|
XM_011538185.1:c.856-1255A>C
|
XP_011536487.1:n.856-1255A>C
|
|
XM_011538186.1:c.407A>C
|
XP_011536488.1:p.Tyr136Ser
|
|
NM_001164690.2:c.1232A>C
|
NP_001158162.1:p.Tyr411Ser
|
|
NM_001164691.2:c.1140+297A>C
|
NP_001158163.1:n.1140+297A>C
|
|
NM_020547.3:c.1232A>C
MANE Select
|
NP_065434.1:p.Tyr411Ser
|
|
XM_011538183.2:c.1201-224A>C
|
XP_011536485.1:n.1201-224A>C
|
|
XM_011538184.2:c.1220+277A>C
|
XP_011536486.1:n.1220+277A>C
|
|
XM_011538186.3:c.407A>C
|
XP_011536488.1:p.Tyr136Ser
|
|
XM_017019179.2:c.1292A>C
|
XP_016874668.1:p.Tyr431Ser
|
|
XM_024448938.1:c.1143+297A>C
|
XP_024304706.1:n.1143+297A>C
|
|
XR_002957309.1:n.1200A>C
|
|
|
XR_002957310.1:n.1109-224A>C
|
|
|
XR_002957311.1:n.1200A>C
|
|
|
XR_002957312.1:n.1108+297A>C
|
|
|