ENST00000261769.10:c.1766A>G
MANE Select
|
ENSP00000261769.4:p.Asn589Ser
|
|
ENST00000261769.9:c.1766A>G
|
ENSP00000261769.4:p.Asn589Ser
|
|
ENST00000422392.6:c.1583A>G
|
ENSP00000414946.2:p.Asn528Ser
|
|
ENST00000562836.5:n.1837A>G
|
|
|
ENST00000566510.5:c.*432A>G
|
ENSP00000458139.1:n.*432A>G
|
|
ENST00000566612.5:c.*6A>G
|
ENSP00000454782.1:n.*6A>G
|
|
ENST00000611625.4:c.1829A>G
|
ENSP00000481063.1:p.Asn610Ser
|
|
ENST00000612417.4:c.1766A>G
|
ENSP00000478360.1:p.Asn589Ser
|
|
ENST00000621016.4:c.1766A>G
|
ENSP00000480664.1:p.Asn589Ser
|
|
NM_004360.3:c.1766A>G , LRG_301t1:c.1766A>G
|
NP_004351.1:p.Asn589Ser
|
|
XM_011523488.1:c.1031A>G
|
XP_011521790.1:p.Asn344Ser
|
|
XM_011523489.1:c.1031A>G
|
XP_011521791.1:p.Asn344Ser
|
|
NM_001317184.1:c.1583A>G
|
NP_001304113.1:p.Asn528Ser
|
|
NM_001317185.1:c.218A>G
|
NP_001304114.1:p.Asn73Ser
|
|
NM_001317186.1:c.-200A>G
|
NP_001304115.1:n.-200A>G
|
|
NM_004360.4:c.1766A>G
|
NP_004351.1:p.Asn589Ser
|
|
NM_004360.5:c.1766A>G
MANE Select
|
NP_004351.1:p.Asn589Ser
|
|
NM_001317184.2:c.1583A>G
|
NP_001304113.1:p.Asn528Ser
|
|
NM_001317185.2:c.218A>G
|
NP_001304114.1:p.Asn73Ser
|
|
NM_001317186.2:c.-200A>G
|
NP_001304115.1:n.-200A>G
|
|