|
ENST00000703936.1:c.2766A>T
|
ENSP00000515567.1:p.Lys922Asn
|
|
|
ENST00000703937.1:c.*1827A>T
|
ENSP00000515568.1:n.*1827A>T
|
|
|
ENST00000326739.9:c.726A>T
MANE Select
|
ENSP00000321584.4:p.Lys242Asn
|
|
|
ENST00000429182.6:c.726A>T
|
ENSP00000393525.2:p.Lys242Asn
|
|
|
ENST00000442157.2:c.651A>T
|
ENSP00000403502.2:p.Lys217Asn
|
|
|
ENST00000462980.2:n.1241A>T
|
|
|
|
ENST00000472328.2:n.792A>T
|
|
|
|
ENST00000491610.2:n.686A>T
|
|
|
|
ENST00000676607.1:n.1022A>T
|
|
|
|
ENST00000676627.1:n.1456A>T
|
|
|
|
ENST00000676708.1:n.2006A>T
|
|
|
|
ENST00000676864.1:n.1875A>T
|
|
|
|
ENST00000677010.1:c.762A>T
|
ENSP00000503089.1:p.Lys254Asn
|
|
|
ENST00000677108.1:n.2632A>T
|
|
|
|
ENST00000677168.1:n.1198A>T
|
|
|
|
ENST00000677185.1:n.1289A>T
|
|
|
|
ENST00000677205.1:n.1510A>T
|
|
|
|
ENST00000677344.1:n.2000A>T
|
|
|
|
ENST00000677480.1:c.*403A>T
|
ENSP00000504378.1:n.*403A>T
|
|
|
ENST00000677519.1:n.1436A>T
|
|
|
|
ENST00000677593.1:n.1282A>T
|
|
|
|
ENST00000677740.1:n.2231A>T
|
|
|
|
ENST00000677991.1:n.1899A>T
|
|
|
|
ENST00000678001.1:n.1219A>T
|
|
|
|
ENST00000678085.1:n.1282A>T
|
|
|
|
ENST00000678177.1:n.2575A>T
|
|
|
|
ENST00000678603.1:n.1804A>T
|
|
|
|
ENST00000678724.1:c.651A>T
|
ENSP00000503874.1:p.Lys217Asn
|
|
|
ENST00000678920.1:n.884A>T
|
|
|
|
ENST00000679019.1:n.1496A>T
|
|
|
|
ENST00000679117.1:c.*541A>T
|
ENSP00000503240.1:n.*541A>T
|
|
|
ENST00000679339.1:n.1567A>T
|
|
|
|
ENST00000326739.8:c.726A>T
|
ENSP00000321584.4:p.Lys242Asn
|
|
|
ENST00000429182.5:c.520A>T
|
|
|
|
ENST00000442157.1:c.651A>T
|
ENSP00000403502.1:p.Lys217Asn
|
|
|
ENST00000462980.1:n.628A>T
|
|
|
|
ENST00000491610.1:n.686A>T
|
|
|
|
NM_000884.2:c.726A>T
|
NP_000875.2:p.Lys242Asn
|
|
|
XM_006713128.2:c.936A>T
|
XP_006713191.1:p.Lys312Asn
|
|
|
XM_006713128.3:c.936A>T
|
XP_006713191.1:p.Lys312Asn
|
|
|
XM_017006349.1:c.861A>T
|
XP_016861838.1:p.Lys287Asn
|
|
|
XM_017006350.1:c.861A>T
|
XP_016861839.1:p.Lys287Asn
|
|
|
NM_000884.3:c.726A>T
MANE Select
|
NP_000875.2:p.Lys242Asn
|
|
