ENST00000558767.6:c.451A>G
|
ENSP00000507680.1:p.Asn151Asp
|
|
ENST00000682012.1:n.526A>G
|
|
|
ENST00000683593.1:n.2114A>G
|
|
|
ENST00000684363.1:c.365-60A>G
|
ENSP00000507314.1:n.365-60A>G
|
|
ENST00000684569.1:n.496A>G
|
|
|
ENST00000561421.6:c.451A>G
MANE Select
|
ENSP00000453347.2:p.Asn151Asp
|
|
ENST00000646551.1:n.1938A>G
|
|
|
ENST00000261755.9:c.451A>G
|
ENSP00000261755.5:p.Asn151Asp
|
|
ENST00000407106.5:c.451A>G
|
ENSP00000385080.1:p.Asn151Asp
|
|
ENST00000537726.5:n.597A>G
|
|
|
ENST00000539156.5:c.241A>G
|
ENSP00000454271.1:p.Asn81Asp
|
|
ENST00000558022.5:c.451A>G
|
ENSP00000453152.1:p.Asn151Asp
|
|
ENST00000558627.1:n.379A>G
|
|
|
ENST00000558767.5:n.712A>G
|
|
|
ENST00000561369.1:n.595A>G
|
|
|
ENST00000561421.5:c.451A>G
|
ENSP00000453347.1:p.Asn151Asp
|
|
NM_000137.2:c.451A>G
|
NP_000128.1:p.Asn151Asp
|
|
XM_024449872.1:c.451A>G
|
XP_024305640.1:p.Asn151Asp
|
|
NM_000137.4:c.451A>G
MANE Select
|
NP_000128.1:p.Asn151Asp
|
|
NM_001374377.1:c.451A>G
|
NP_001361306.1:p.Asn151Asp
|
|
NM_001374380.1:c.451A>G
|
NP_001361309.1:p.Asn151Asp
|
|