ENST00000697149.1:c.1400A>T
|
ENSP00000513138.1:n.1400A>T
|
|
ENST00000697150.1:c.1458A>T
|
ENSP00000513139.1:n.1458A>T
|
|
ENST00000697151.1:c.1391A>T
|
ENSP00000513140.1:n.1391A>T
|
|
ENST00000697164.1:c.1471A>T
|
ENSP00000513153.1:p.Asn491Tyr
|
|
ENST00000697165.1:c.1258A>T
|
ENSP00000513154.1:p.Asn420Tyr
|
|
ENST00000347310.10:c.1561A>T
MANE Select
|
ENSP00000321345.5:p.Asn521Tyr
|
|
ENST00000637002.1:c.952A>T
|
ENSP00000490340.1:p.Asn318Tyr
|
|
ENST00000347310.9:c.1561A>T
|
ENSP00000321345.5:p.Asn521Tyr
|
|
ENST00000395227.2:c.355A>T
|
ENSP00000378652.2:p.Asn119Tyr
|
|
ENST00000425614.3:c.796A>T
|
ENSP00000387640.2:p.Asn266Tyr
|
|
ENST00000473881.2:c.*387A>T
|
ENSP00000486667.1:n.*387A>T
|
|
NM_144701.2:c.1561A>T
|
NP_653302.2:p.Asn521Tyr
|
|
XM_005270516.2:c.799A>T
|
XP_005270573.1:p.Asn267Tyr
|
|
XM_011540789.1:c.1651A>T
|
XP_011539091.1:p.Asn551Tyr
|
|
XM_011540790.1:c.1561A>T
|
XP_011539092.1:p.Asn521Tyr
|
|
XM_011540791.1:c.1561A>T
|
XP_011539093.1:p.Asn521Tyr
|
|
XM_011540790.3:c.1561A>T
|
XP_011539092.1:p.Asn521Tyr
|
|
XM_011540791.3:c.1561A>T
|
XP_011539093.1:p.Asn521Tyr
|
|
XR_001736993.1:n.1641A>T
|
|
|
NM_144701.3:c.1561A>T
MANE Select
|
NP_653302.2:p.Asn521Tyr
|
|