ENST00000281928.9:c.5089A>C
MANE Select
|
ENSP00000281928.3:p.Asn1697His
|
|
ENST00000549786.2:c.4517A>C
|
|
|
ENST00000648379.1:n.3457A>C
|
|
|
ENST00000648737.1:n.4853A>C
|
|
|
ENST00000648825.1:n.1829A>C
|
|
|
ENST00000648916.1:n.3100A>C
|
|
|
ENST00000649146.1:n.2332A>C
|
|
|
ENST00000649607.1:c.3273A>C
|
|
|
ENST00000649775.1:c.1578A>C
|
|
|
ENST00000650226.1:c.5089A>C
|
ENSP00000496981.1:p.Asn1697His
|
|
ENST00000281928.7:c.5089A>C
|
ENSP00000281928.3:p.Asn1697His
|
|
ENST00000549786.1:c.453A>C
|
|
|
ENST00000552340.1:c.121A>C
|
ENSP00000449876.1:p.Asn41His
|
|
NM_015335.4:c.5089A>C
|
NP_056150.1:p.Asn1697His
|
|
XM_011538080.1:c.5089A>C
|
XP_011536382.1:p.Asn1697His
|
|
XM_011538081.1:c.5086A>C
|
XP_011536383.1:p.Asn1696His
|
|
XM_011538082.1:c.5059A>C
|
XP_011536384.1:p.Asn1687His
|
|
XM_011538080.2:c.5089A>C
|
XP_011536382.1:p.Asn1697His
|
|
XM_011538081.2:c.5086A>C
|
XP_011536383.1:p.Asn1696His
|
|
XM_011538082.2:c.5059A>C
|
XP_011536384.1:p.Asn1687His
|
|
XM_017019090.1:c.5086A>C
|
XP_016874579.1:p.Asn1696His
|
|
NM_015335.5:c.5089A>C
MANE Select
|
NP_056150.1:p.Asn1697His
|
|