ENST00000281928.9:c.5089A>T
MANE Select
|
ENSP00000281928.3:p.Asn1697Tyr
|
|
ENST00000549786.2:c.4517A>T
|
|
|
ENST00000648379.1:n.3457A>T
|
|
|
ENST00000648737.1:n.4853A>T
|
|
|
ENST00000648825.1:n.1829A>T
|
|
|
ENST00000648916.1:n.3100A>T
|
|
|
ENST00000649146.1:n.2332A>T
|
|
|
ENST00000649607.1:c.3273A>T
|
|
|
ENST00000649775.1:c.1578A>T
|
|
|
ENST00000650226.1:c.5089A>T
|
ENSP00000496981.1:p.Asn1697Tyr
|
|
ENST00000281928.7:c.5089A>T
|
ENSP00000281928.3:p.Asn1697Tyr
|
|
ENST00000549786.1:c.453A>T
|
|
|
ENST00000552340.1:c.121A>T
|
ENSP00000449876.1:p.Asn41Tyr
|
|
NM_015335.4:c.5089A>T
|
NP_056150.1:p.Asn1697Tyr
|
|
XM_011538080.1:c.5089A>T
|
XP_011536382.1:p.Asn1697Tyr
|
|
XM_011538081.1:c.5086A>T
|
XP_011536383.1:p.Asn1696Tyr
|
|
XM_011538082.1:c.5059A>T
|
XP_011536384.1:p.Asn1687Tyr
|
|
XM_011538080.2:c.5089A>T
|
XP_011536382.1:p.Asn1697Tyr
|
|
XM_011538081.2:c.5086A>T
|
XP_011536383.1:p.Asn1696Tyr
|
|
XM_011538082.2:c.5059A>T
|
XP_011536384.1:p.Asn1687Tyr
|
|
XM_017019090.1:c.5086A>T
|
XP_016874579.1:p.Asn1696Tyr
|
|
NM_015335.5:c.5089A>T
MANE Select
|
NP_056150.1:p.Asn1697Tyr
|
|