ENST00000435817.7:c.779C>T
MANE Select
|
ENSP00000399259.2:p.Ala260Val
|
|
ENST00000435817.6:c.779C>T
|
ENSP00000399259.2:p.Ala260Val
|
|
ENST00000522126.5:c.551C>T
|
ENSP00000427796.1:p.Ala184Val
|
|
ENST00000522386.1:n.385C>T
|
|
|
ENST00000522763.5:n.83C>T
|
|
|
ENST00000522783.5:c.773C>T
|
ENSP00000428677.1:p.Ala258Val
|
|
ENST00000523856.5:n.37C>T
|
|
|
NM_033449.2:c.779C>T
|
NP_258260.1:p.Ala260Val
|
|
XM_005268524.3:c.773C>T
|
XP_005268581.1:p.Ala258Val
|
|
XM_006714803.2:c.650C>T
|
XP_006714866.1:p.Ala217Val
|
|
XM_011537698.1:c.779C>T
|
XP_011536000.1:p.Ala260Val
|
|
XM_011537699.1:c.779C>T
|
XP_011536001.1:p.Ala260Val
|
|
XM_011537700.1:c.779C>T
|
XP_011536002.1:p.Ala260Val
|
|
XM_011537701.1:c.779C>T
|
XP_011536003.1:p.Ala260Val
|
|
XR_427781.2:n.833C>T
|
|
|
XR_944338.1:n.839C>T
|
|
|
XR_944339.1:n.839C>T
|
|
|
XM_005268524.5:c.773C>T
|
XP_005268581.1:p.Ala258Val
|
|
XM_006714803.4:c.650C>T
|
XP_006714866.1:p.Ala217Val
|
|
XM_011537698.3:c.779C>T
|
XP_011536000.1:p.Ala260Val
|
|
XM_011537700.3:c.779C>T
|
XP_011536002.1:p.Ala260Val
|
|
XM_011537701.3:c.779C>T
|
XP_011536003.1:p.Ala260Val
|
|
XM_017010013.2:c.779C>T
|
XP_016865502.1:p.Ala260Val
|
|
XR_002956197.1:n.775C>T
|
|
|
XR_427781.4:n.775C>T
|
|
|
XR_944338.3:n.854C>T
|
|
|
XR_944339.3:n.854C>T
|
|
|
NM_033449.3:c.779C>T
MANE Select
|
NP_258260.1:p.Ala260Val
|
|