ENST00000682422.1:n.866G>A
|
|
|
ENST00000682545.1:c.*291G>A
|
ENSP00000508402.1:n.*291G>A
|
|
ENST00000682887.1:c.1686G>A
|
ENSP00000506946.1:n.1686G>A
|
|
ENST00000683302.1:c.1216G>A
|
ENSP00000507885.1:p.Asp406Asn
|
|
ENST00000683557.1:c.*117G>A
|
ENSP00000508029.1:n.*117G>A
|
|
ENST00000367282.6:c.1285G>A
MANE Select
|
ENSP00000356251.4:p.Asp429Asn
|
|
ENST00000367282.5:c.1285G>A
|
ENSP00000356251.4:p.Asp429Asn
|
|
NM_004767.3:c.1285G>A
|
NP_004758.3:p.Asp429Asn
|
|
XM_011510158.1:c.724G>A
|
XP_011508460.1:p.Asp242Asn
|
|
NM_004767.4:c.1285G>A
|
NP_004758.3:p.Asp429Asn
|
|
XM_011510158.2:c.724G>A
|
XP_011508460.1:p.Asp242Asn
|
|
NM_004767.5:c.1285G>A
MANE Select
|
NP_004758.3:p.Asp429Asn
|
|