|
ENST00000421709.2:c.259C>T
|
ENSP00000388120.2:p.His87Tyr
|
|
|
ENST00000700228.1:c.319C>T
|
ENSP00000514865.1:p.His107Tyr
|
|
|
ENST00000700231.1:c.448C>T
|
ENSP00000514868.1:p.His150Tyr
|
|
|
ENST00000339562.9:c.448C>T
MANE Select
|
ENSP00000344479.4:p.His150Tyr
|
|
|
ENST00000675870.1:c.259C>T
|
ENSP00000502739.1:p.His87Tyr
|
|
|
ENST00000339562.8:c.448C>T
|
ENSP00000344479.4:p.His150Tyr
|
|
|
ENST00000406048.2:c.208+175C>T
|
|
|
|
ENST00000409108.6:c.448C>T
|
ENSP00000386993.2:p.His150Tyr
|
|
|
ENST00000409572.5:c.448C>T
|
ENSP00000386747.1:p.His150Tyr
|
|
|
ENST00000417764.5:c.259C>T
|
ENSP00000415632.1:p.His87Tyr
|
|
|
ENST00000417972.5:c.259C>T
|
ENSP00000394671.1:p.His87Tyr
|
|
|
ENST00000421709.1:c.259C>T
|
ENSP00000388120.1:p.His87Tyr
|
|
|
ENST00000424077.1:c.448C>T
|
ENSP00000406808.1:p.His150Tyr
|
|
|
ENST00000426264.5:c.259C>T
|
ENSP00000389986.1:p.His87Tyr
|
|
|
ENST00000429376.5:c.259C>T
|
ENSP00000410952.1:p.His87Tyr
|
|
|
NM_006186.3:c.448C>T
|
NP_006177.1:p.His150Tyr
|
|
|
XM_005246621.2:c.481C>T
|
XP_005246678.1:p.His161Tyr
|
|
|
XM_005246622.2:c.259C>T
|
XP_005246679.1:p.His87Tyr
|
|
|
XM_005246623.1:c.259C>T
|
XP_005246680.1:p.His87Tyr
|
|
|
XM_006712553.2:c.481C>T
|
XP_006712616.1:p.His161Tyr
|
|
|
XM_011511246.1:c.481C>T
|
XP_011509548.1:p.His161Tyr
|
|
|
XR_427087.2:n.2654C>T
|
|
|
|
NM_173173.2:c.259C>T
|
NP_775265.1:p.His87Tyr
|
|
|
XM_005246621.4:c.481C>T
|
XP_005246678.1:p.His161Tyr
|
|
|
XM_006712553.4:c.481C>T
|
XP_006712616.1:p.His161Tyr
|
|
|
XM_011511246.2:c.481C>T
|
XP_011509548.1:p.His161Tyr
|
|
|
XM_017004219.2:c.448C>T
|
XP_016859708.1:p.His150Tyr
|
|
|
XM_017004220.2:c.448C>T
|
XP_016859709.1:p.His150Tyr
|
|
|
XR_001738751.2:n.816C>T
|
|
|
|
XR_001738752.2:n.638C>T
|
|
|
|
XR_427087.4:n.695C>T
|
|
|
|
NM_006186.4:c.448C>T
MANE Select
|
NP_006177.1:p.His150Tyr
|
|
|
NM_173173.3:c.259C>T
|
NP_775265.1:p.His87Tyr
|
|
