ENST00000527168.6:n.394A>T
|
|
|
ENST00000529110.2:c.379A>T
|
ENSP00000435349.2:p.Asn127Tyr
|
|
ENST00000529957.6:n.353A>T
|
|
|
ENST00000683366.1:c.*27A>T
|
ENSP00000507283.1:n.*27A>T
|
|
ENST00000683887.1:c.343A>T
|
ENSP00000506886.1:p.Asn115Tyr
|
|
ENST00000684100.1:n.289A>T
|
|
|
ENST00000684126.1:n.353A>T
|
|
|
ENST00000684688.1:n.920A>T
|
|
|
ENST00000204679.9:c.295A>T
MANE Select
|
ENSP00000204679.4:p.Asn99Tyr
|
|
ENST00000204679.8:c.295A>T
|
ENSP00000204679.4:p.Asn99Tyr
|
|
ENST00000526820.5:c.*197A>T
|
ENSP00000434413.1:n.*197A>T
|
|
ENST00000527076.1:n.1311A>T
|
|
|
ENST00000527168.5:n.331A>T
|
|
|
ENST00000529110.1:c.362A>T
|
|
|
ENST00000529957.5:n.394A>T
|
|
|
NM_032520.4:c.295A>T
|
NP_115909.1:p.Asn99Tyr
|
|
XM_017023782.1:c.343A>T
|
XP_016879271.1:p.Asn115Tyr
|
|
XM_017023783.1:c.-66A>T
|
XP_016879272.1:n.-66A>T
|
|
NM_032520.5:c.295A>T
MANE Select
|
NP_115909.1:p.Asn99Tyr
|
|