ENST00000271651.8:c.490C>A
MANE Select
|
ENSP00000271651.3:p.Pro164Thr
|
|
ENST00000443913.2:c.667C>A
|
ENSP00000405083.2:p.Pro223Thr
|
|
ENST00000480670.2:n.3559C>A
|
|
|
ENST00000676680.1:c.490C>A
|
ENSP00000503270.1:p.Pro164Thr
|
|
ENST00000676716.1:c.367C>A
|
ENSP00000504737.1:p.Pro123Thr
|
|
ENST00000676751.1:c.490C>A
|
ENSP00000502964.1:p.Pro164Thr
|
|
ENST00000676824.1:c.490C>A
|
ENSP00000504176.1:p.Pro164Thr
|
|
ENST00000676966.1:c.490C>A
|
ENSP00000503723.1:p.Pro164Thr
|
|
ENST00000676970.1:c.490C>A
|
ENSP00000503832.1:p.Pro164Thr
|
|
ENST00000677330.1:n.2316C>A
|
|
|
ENST00000677611.1:n.342C>A
|
|
|
ENST00000677887.1:c.532C>A
|
ENSP00000503876.1:p.Pro178Thr
|
|
ENST00000678275.1:c.*382C>A
|
ENSP00000504796.1:n.*382C>A
|
|
ENST00000678337.1:c.526C>A
|
ENSP00000504759.1:p.Pro176Thr
|
|
ENST00000678725.1:n.1467C>A
|
|
|
ENST00000679090.1:n.1075C>A
|
|
|
ENST00000679148.1:n.3452C>A
|
|
|
ENST00000679171.1:n.2851C>A
|
|
|
ENST00000679260.1:c.399+1712C>A
|
ENSP00000504534.1:n.399+1712C>A
|
|
ENST00000271651.7:c.490C>A
|
ENSP00000271651.3:p.Pro164Thr
|
|
ENST00000443913.1:c.667C>A
|
ENSP00000405083.1:p.Pro223Thr
|
|
ENST00000480670.1:n.330C>A
|
|
|
NM_000396.3:c.490C>A
|
NP_000387.1:p.Pro164Thr
|
|
NM_000396.4:c.490C>A
MANE Select
|
NP_000387.1:p.Pro164Thr
|
|