ENST00000271651.8:c.486G>T
MANE Select
|
ENSP00000271651.3:p.Leu162=
|
|
ENST00000443913.2:c.663G>T
|
ENSP00000405083.2:p.Leu221=
|
|
ENST00000480670.2:n.3555G>T
|
|
|
ENST00000676680.1:c.486G>T
|
ENSP00000503270.1:p.Leu162=
|
|
ENST00000676716.1:c.363G>T
|
ENSP00000504737.1:p.Leu121=
|
|
ENST00000676751.1:c.486G>T
|
ENSP00000502964.1:p.Leu162=
|
|
ENST00000676824.1:c.486G>T
|
ENSP00000504176.1:p.Leu162=
|
|
ENST00000676966.1:c.486G>T
|
ENSP00000503723.1:p.Leu162=
|
|
ENST00000676970.1:c.486G>T
|
ENSP00000503832.1:p.Leu162=
|
|
ENST00000677330.1:n.2312G>T
|
|
|
ENST00000677611.1:n.338G>T
|
|
|
ENST00000677887.1:c.528G>T
|
ENSP00000503876.1:p.Leu176=
|
|
ENST00000678275.1:c.*378G>T
|
ENSP00000504796.1:n.*378G>T
|
|
ENST00000678337.1:c.522G>T
|
ENSP00000504759.1:p.Leu174=
|
|
ENST00000678725.1:n.1463G>T
|
|
|
ENST00000679090.1:n.1071G>T
|
|
|
ENST00000679148.1:n.3448G>T
|
|
|
ENST00000679171.1:n.2847G>T
|
|
|
ENST00000679260.1:c.399+1708G>T
|
ENSP00000504534.1:n.399+1708G>T
|
|
ENST00000271651.7:c.486G>T
|
ENSP00000271651.3:p.Leu162=
|
|
ENST00000443913.1:c.663G>T
|
ENSP00000405083.1:p.Leu221=
|
|
ENST00000480670.1:n.326G>T
|
|
|
NM_000396.3:c.486G>T
|
NP_000387.1:p.Leu162=
|
|
NM_000396.4:c.486G>T
MANE Select
|
NP_000387.1:p.Leu162=
|
|