ENST00000281928.9:c.5149C>A
MANE Select
|
ENSP00000281928.3:p.His1717Asn
|
|
ENST00000549786.2:c.4577C>A
|
|
|
ENST00000648379.1:n.3517C>A
|
|
|
ENST00000648737.1:n.4913C>A
|
|
|
ENST00000648825.1:n.1889C>A
|
|
|
ENST00000648916.1:n.3160C>A
|
|
|
ENST00000649146.1:n.2392C>A
|
|
|
ENST00000649607.1:c.3333C>A
|
|
|
ENST00000649775.1:c.1638C>A
|
|
|
ENST00000650226.1:c.5149C>A
|
ENSP00000496981.1:p.His1717Asn
|
|
ENST00000281928.7:c.5149C>A
|
ENSP00000281928.3:p.His1717Asn
|
|
ENST00000549786.1:c.513C>A
|
|
|
ENST00000552340.1:c.181C>A
|
ENSP00000449876.1:p.His61Asn
|
|
NM_015335.4:c.5149C>A
|
NP_056150.1:p.His1717Asn
|
|
XM_011538080.1:c.5149C>A
|
XP_011536382.1:p.His1717Asn
|
|
XM_011538081.1:c.5146C>A
|
XP_011536383.1:p.His1716Asn
|
|
XM_011538082.1:c.5119C>A
|
XP_011536384.1:p.His1707Asn
|
|
XM_011538080.2:c.5149C>A
|
XP_011536382.1:p.His1717Asn
|
|
XM_011538081.2:c.5146C>A
|
XP_011536383.1:p.His1716Asn
|
|
XM_011538082.2:c.5119C>A
|
XP_011536384.1:p.His1707Asn
|
|
XM_017019090.1:c.5146C>A
|
XP_016874579.1:p.His1716Asn
|
|
NM_015335.5:c.5149C>A
MANE Select
|
NP_056150.1:p.His1717Asn
|
|