ENST00000271651.8:c.450C>T
MANE Select
|
ENSP00000271651.3:p.Gly150=
|
|
ENST00000443913.2:c.627C>T
|
ENSP00000405083.2:p.Gly209=
|
|
ENST00000480670.2:n.3519C>T
|
|
|
ENST00000676680.1:c.450C>T
|
ENSP00000503270.1:p.Gly150=
|
|
ENST00000676716.1:c.327C>T
|
ENSP00000504737.1:p.Gly109=
|
|
ENST00000676751.1:c.450C>T
|
ENSP00000502964.1:p.Gly150=
|
|
ENST00000676824.1:c.450C>T
|
ENSP00000504176.1:p.Gly150=
|
|
ENST00000676966.1:c.450C>T
|
ENSP00000503723.1:p.Gly150=
|
|
ENST00000676970.1:c.450C>T
|
ENSP00000503832.1:p.Gly150=
|
|
ENST00000677330.1:n.2276C>T
|
|
|
ENST00000677611.1:n.302C>T
|
|
|
ENST00000677887.1:c.492C>T
|
ENSP00000503876.1:p.Gly164=
|
|
ENST00000678275.1:c.*342C>T
|
ENSP00000504796.1:n.*342C>T
|
|
ENST00000678337.1:c.486C>T
|
ENSP00000504759.1:p.Gly162=
|
|
ENST00000678725.1:n.1427C>T
|
|
|
ENST00000679090.1:n.1035C>T
|
|
|
ENST00000679148.1:n.3412C>T
|
|
|
ENST00000679171.1:n.2811C>T
|
|
|
ENST00000679260.1:c.399+1672C>T
|
ENSP00000504534.1:n.399+1672C>T
|
|
ENST00000271651.7:c.450C>T
|
ENSP00000271651.3:p.Gly150=
|
|
ENST00000443913.1:c.627C>T
|
ENSP00000405083.1:p.Gly209=
|
|
ENST00000480670.1:n.290C>T
|
|
|
NM_000396.3:c.450C>T
|
NP_000387.1:p.Gly150=
|
|
NM_000396.4:c.450C>T
MANE Select
|
NP_000387.1:p.Gly150=
|
|