ENST00000271651.8:c.480A>G
MANE Select
|
ENSP00000271651.3:p.Leu160=
|
|
ENST00000443913.2:c.657A>G
|
ENSP00000405083.2:p.Leu219=
|
|
ENST00000480670.2:n.3549A>G
|
|
|
ENST00000676680.1:c.480A>G
|
ENSP00000503270.1:p.Leu160=
|
|
ENST00000676716.1:c.357A>G
|
ENSP00000504737.1:p.Leu119=
|
|
ENST00000676751.1:c.480A>G
|
ENSP00000502964.1:p.Leu160=
|
|
ENST00000676824.1:c.480A>G
|
ENSP00000504176.1:p.Leu160=
|
|
ENST00000676966.1:c.480A>G
|
ENSP00000503723.1:p.Leu160=
|
|
ENST00000676970.1:c.480A>G
|
ENSP00000503832.1:p.Leu160=
|
|
ENST00000677330.1:n.2306A>G
|
|
|
ENST00000677611.1:n.332A>G
|
|
|
ENST00000677887.1:c.522A>G
|
ENSP00000503876.1:p.Leu174=
|
|
ENST00000678275.1:c.*372A>G
|
ENSP00000504796.1:n.*372A>G
|
|
ENST00000678337.1:c.516A>G
|
ENSP00000504759.1:p.Leu172=
|
|
ENST00000678725.1:n.1457A>G
|
|
|
ENST00000679090.1:n.1065A>G
|
|
|
ENST00000679148.1:n.3442A>G
|
|
|
ENST00000679171.1:n.2841A>G
|
|
|
ENST00000679260.1:c.399+1702A>G
|
ENSP00000504534.1:n.399+1702A>G
|
|
ENST00000271651.7:c.480A>G
|
ENSP00000271651.3:p.Leu160=
|
|
ENST00000443913.1:c.657A>G
|
ENSP00000405083.1:p.Leu219=
|
|
ENST00000480670.1:n.320A>G
|
|
|
NM_000396.3:c.480A>G
|
NP_000387.1:p.Leu160=
|
|
NM_000396.4:c.480A>G
MANE Select
|
NP_000387.1:p.Leu160=
|
|