ENST00000435817.7:c.762C>T
MANE Select
|
ENSP00000399259.2:p.His254=
|
|
ENST00000435817.6:c.762C>T
|
ENSP00000399259.2:p.His254=
|
|
ENST00000522126.5:c.534C>T
|
ENSP00000427796.1:p.His178=
|
|
ENST00000522386.1:n.368C>T
|
|
|
ENST00000522763.5:n.66C>T
|
|
|
ENST00000522783.5:c.756C>T
|
ENSP00000428677.1:p.His252=
|
|
ENST00000523856.5:n.20C>T
|
|
|
NM_033449.2:c.762C>T
|
NP_258260.1:p.His254=
|
|
XM_005268524.3:c.756C>T
|
XP_005268581.1:p.His252=
|
|
XM_006714803.2:c.633C>T
|
XP_006714866.1:p.His211=
|
|
XM_011537698.1:c.762C>T
|
XP_011536000.1:p.His254=
|
|
XM_011537699.1:c.762C>T
|
XP_011536001.1:p.His254=
|
|
XM_011537700.1:c.762C>T
|
XP_011536002.1:p.His254=
|
|
XM_011537701.1:c.762C>T
|
XP_011536003.1:p.His254=
|
|
XR_427781.2:n.816C>T
|
|
|
XR_944338.1:n.822C>T
|
|
|
XR_944339.1:n.822C>T
|
|
|
XM_005268524.5:c.756C>T
|
XP_005268581.1:p.His252=
|
|
XM_006714803.4:c.633C>T
|
XP_006714866.1:p.His211=
|
|
XM_011537698.3:c.762C>T
|
XP_011536000.1:p.His254=
|
|
XM_011537700.3:c.762C>T
|
XP_011536002.1:p.His254=
|
|
XM_011537701.3:c.762C>T
|
XP_011536003.1:p.His254=
|
|
XM_017010013.2:c.762C>T
|
XP_016865502.1:p.His254=
|
|
XR_002956197.1:n.758C>T
|
|
|
XR_427781.4:n.758C>T
|
|
|
XR_944338.3:n.837C>T
|
|
|
XR_944339.3:n.837C>T
|
|
|
NM_033449.3:c.762C>T
MANE Select
|
NP_258260.1:p.His254=
|
|