ENST00000527168.6:n.445A>T
|
|
|
ENST00000529110.2:c.430A>T
|
ENSP00000435349.2:p.Asn144Tyr
|
|
ENST00000529957.6:n.404A>T
|
|
|
ENST00000683366.1:c.*78A>T
|
ENSP00000507283.1:n.*78A>T
|
|
ENST00000683887.1:c.394A>T
|
ENSP00000506886.1:p.Asn132Tyr
|
|
ENST00000684100.1:n.340A>T
|
|
|
ENST00000684126.1:n.404A>T
|
|
|
ENST00000684688.1:n.971A>T
|
|
|
ENST00000204679.9:c.346A>T
MANE Select
|
ENSP00000204679.4:p.Asn116Tyr
|
|
ENST00000204679.8:c.346A>T
|
ENSP00000204679.4:p.Asn116Tyr
|
|
ENST00000526820.5:c.*248A>T
|
ENSP00000434413.1:n.*248A>T
|
|
ENST00000527076.1:n.1362A>T
|
|
|
ENST00000527168.5:n.382A>T
|
|
|
ENST00000529110.1:c.413A>T
|
|
|
ENST00000529957.5:n.445A>T
|
|
|
NM_032520.4:c.346A>T
|
NP_115909.1:p.Asn116Tyr
|
|
XM_017023782.1:c.394A>T
|
XP_016879271.1:p.Asn132Tyr
|
|
XM_017023783.1:c.-15A>T
|
XP_016879272.1:n.-15A>T
|
|
NM_032520.5:c.346A>T
MANE Select
|
NP_115909.1:p.Asn116Tyr
|
|