ENST00000271651.8:c.514T>C
MANE Select
|
ENSP00000271651.3:p.Ser172Pro
|
|
ENST00000443913.2:c.691T>C
|
ENSP00000405083.2:p.Ser231Pro
|
|
ENST00000480670.2:n.3583T>C
|
|
|
ENST00000676680.1:c.514T>C
|
ENSP00000503270.1:p.Ser172Pro
|
|
ENST00000676716.1:c.391T>C
|
ENSP00000504737.1:p.Ser131Pro
|
|
ENST00000676751.1:c.514T>C
|
ENSP00000502964.1:p.Ser172Pro
|
|
ENST00000676824.1:c.514T>C
|
ENSP00000504176.1:p.Ser172Pro
|
|
ENST00000676966.1:c.514T>C
|
ENSP00000503723.1:p.Ser172Pro
|
|
ENST00000676970.1:c.514T>C
|
ENSP00000503832.1:p.Ser172Pro
|
|
ENST00000677330.1:n.2340T>C
|
|
|
ENST00000677611.1:n.366T>C
|
|
|
ENST00000677887.1:c.556T>C
|
ENSP00000503876.1:p.Ser186Pro
|
|
ENST00000678275.1:c.*406T>C
|
ENSP00000504796.1:n.*406T>C
|
|
ENST00000678337.1:c.550T>C
|
ENSP00000504759.1:p.Ser184Pro
|
|
ENST00000678725.1:n.1491T>C
|
|
|
ENST00000679090.1:n.1099T>C
|
|
|
ENST00000679148.1:n.3476T>C
|
|
|
ENST00000679171.1:n.2875T>C
|
|
|
ENST00000679260.1:c.399+1736T>C
|
ENSP00000504534.1:n.399+1736T>C
|
|
ENST00000271651.7:c.514T>C
|
ENSP00000271651.3:p.Ser172Pro
|
|
ENST00000443913.1:c.691T>C
|
ENSP00000405083.1:p.Ser231Pro
|
|
ENST00000480670.1:n.354T>C
|
|
|
NM_000396.3:c.514T>C
|
NP_000387.1:p.Ser172Pro
|
|
NM_000396.4:c.514T>C
MANE Select
|
NP_000387.1:p.Ser172Pro
|
|