ENST00000261819.8:c.1793C>A
MANE Select
|
ENSP00000261819.3:p.Thr598Asn
|
|
ENST00000261819.7:c.1793C>A
|
ENSP00000261819.3:p.Thr598Asn
|
|
ENST00000441917.6:c.1457C>A
|
ENSP00000415061.2:p.Thr486Asn
|
|
ENST00000534976.5:n.2525C>A
|
|
|
ENST00000535482.1:c.791C>A
|
ENSP00000438754.1:p.Thr264Asn
|
|
ENST00000535641.5:n.2004C>A
|
|
|
ENST00000539079.5:c.1117C>A
|
|
|
ENST00000541887.5:c.1754C>A
|
ENSP00000439875.1:p.Thr585Asn
|
|
ENST00000544314.5:n.911C>A
|
|
|
ENST00000545218.5:n.989-26C>A
|
|
|
NM_001137559.1:c.1457C>A
|
NP_001131031.1:p.Thr486Asn
|
|
NM_016237.4:c.1793C>A
|
NP_057321.2:p.Thr598Asn
|
|
XM_005253900.2:c.1754C>A
|
XP_005253957.1:p.Thr585Asn
|
|
XM_006719449.1:c.599C>A
|
XP_006719512.1:p.Thr200Asn
|
|
NM_001330489.1:c.1754C>A
|
NP_001317418.1:p.Thr585Asn
|
|
XM_017019423.2:c.599C>A
|
XP_016874912.1:p.Thr200Asn
|
|
XM_017019424.2:c.599C>A
|
XP_016874913.1:p.Thr200Asn
|
|
NM_016237.5:c.1793C>A
MANE Select
|
NP_057321.2:p.Thr598Asn
|
|
NM_001330489.2:c.1754C>A
|
NP_001317418.1:p.Thr585Asn
|
|