ENST00000271651.8:c.547A>T
MANE Select
|
ENSP00000271651.3:p.Thr183Ser
|
|
ENST00000443913.2:c.724A>T
|
ENSP00000405083.2:p.Thr242Ser
|
|
ENST00000480670.2:n.3616A>T
|
|
|
ENST00000676680.1:c.547A>T
|
ENSP00000503270.1:p.Thr183Ser
|
|
ENST00000676716.1:c.424A>T
|
ENSP00000504737.1:p.Thr142Ser
|
|
ENST00000676751.1:c.547A>T
|
ENSP00000502964.1:p.Thr183Ser
|
|
ENST00000676824.1:c.547A>T
|
ENSP00000504176.1:p.Thr183Ser
|
|
ENST00000676966.1:c.547A>T
|
ENSP00000503723.1:p.Thr183Ser
|
|
ENST00000676970.1:c.547A>T
|
ENSP00000503832.1:p.Thr183Ser
|
|
ENST00000677330.1:n.2373A>T
|
|
|
ENST00000677611.1:n.399A>T
|
|
|
ENST00000677887.1:c.589A>T
|
ENSP00000503876.1:p.Thr197Ser
|
|
ENST00000678275.1:c.*439A>T
|
ENSP00000504796.1:n.*439A>T
|
|
ENST00000678337.1:c.583A>T
|
ENSP00000504759.1:p.Thr195Ser
|
|
ENST00000678725.1:n.1524A>T
|
|
|
ENST00000679090.1:n.1132A>T
|
|
|
ENST00000679148.1:n.3509A>T
|
|
|
ENST00000679171.1:n.2908A>T
|
|
|
ENST00000679260.1:c.399+1769A>T
|
ENSP00000504534.1:n.399+1769A>T
|
|
ENST00000271651.7:c.547A>T
|
ENSP00000271651.3:p.Thr183Ser
|
|
ENST00000443913.1:c.724A>T
|
ENSP00000405083.1:p.Thr242Ser
|
|
ENST00000480670.1:n.387A>T
|
|
|
NM_000396.3:c.547A>T
|
NP_000387.1:p.Thr183Ser
|
|
NM_000396.4:c.547A>T
MANE Select
|
NP_000387.1:p.Thr183Ser
|
|