ENST00000352410.9:c.685A>G
MANE Select
|
ENSP00000318318.6:p.Asn229Asp
|
|
ENST00000323744.10:c.502A>G
|
ENSP00000318192.6:p.Asn168Asp
|
|
ENST00000352410.8:c.685A>G
|
ENSP00000318318.6:p.Asn229Asp
|
|
ENST00000535694.5:c.535A>G
|
ENSP00000440447.1:p.Asn179Asp
|
|
ENST00000561470.5:c.*581A>G
|
ENSP00000454267.1:n.*581A>G
|
|
ENST00000562606.5:c.625A>G
|
ENSP00000457020.1:p.Asn209Asp
|
|
ENST00000562800.5:c.256-1373A>G
|
ENSP00000457619.1:n.256-1373A>G
|
|
ENST00000563422.5:c.685A>G
|
ENSP00000457885.1:p.Asn229Asp
|
|
ENST00000563786.5:c.625A>G
|
ENSP00000455241.1:p.Asn209Asp
|
|
ENST00000564003.5:c.352A>G
|
ENSP00000454312.1:p.Asn118Asp
|
|
ENST00000566377.5:c.685A>G
|
ENSP00000455405.1:p.Asn229Asp
|
|
ENST00000566556.1:n.733A>G
|
|
|
ENST00000567177.1:c.463A>G
|
ENSP00000457013.1:p.Asn155Asp
|
|
ENST00000569931.5:c.625A>G
|
ENSP00000455161.1:p.Asn209Asp
|
|
NM_001289155.1:c.685A>G
|
NP_001276084.1:p.Asn229Asp
|
|
NM_001289156.1:c.535A>G
|
NP_001276085.1:p.Asn179Asp
|
|
NM_001289157.1:c.502A>G
|
NP_001276086.1:p.Asn168Asp
|
|
NM_002435.2:c.685A>G
|
NP_002426.1:p.Asn229Asp
|
|
XM_011521592.1:c.673A>G
|
XP_011519894.1:p.Asn225Asp
|
|
XM_011521593.1:c.625A>G
|
XP_011519895.1:p.Asn209Asp
|
|
NM_001330372.1:c.625A>G
|
NP_001317301.1:p.Asn209Asp
|
|
XM_017022208.1:c.625A>G
|
XP_016877697.1:p.Asn209Asp
|
|
XM_017022209.2:c.535A>G
|
XP_016877698.1:p.Asn179Asp
|
|
NM_002435.3:c.685A>G
MANE Select
|
NP_002426.1:p.Asn229Asp
|
|
NM_001289155.2:c.685A>G
|
NP_001276084.1:p.Asn229Asp
|
|
NM_001289156.2:c.535A>G
|
NP_001276085.1:p.Asn179Asp
|
|
NM_001289157.2:c.502A>G
|
NP_001276086.1:p.Asn168Asp
|
|
NM_001330372.2:c.625A>G
|
NP_001317301.1:p.Asn209Asp
|
|