|
NM_004380.3:c.4615T>A
MANE Select
|
NP_004371.2:p.Tyr1539Asn
|
|
ENST00000262367.10:c.4615T>A
MANE Select
|
ENSP00000262367.5:p.Tyr1539Asn
|
|
NM_001079846.1:c.4501T>A
|
NP_001073315.1:p.Tyr1501Asn
|
|
NM_004380.2:c.4615T>A
|
NP_004371.2:p.Tyr1539Asn
|
|
ENST00000262367.9:c.4615T>A
|
ENSP00000262367.5:p.Tyr1539Asn
|
|
ENST00000382070.7:c.4501T>A
|
ENSP00000371502.3:p.Tyr1501Asn
|
|
ENST00000570939.2:c.3250T>A
|
ENSP00000461002.2:p.Tyr1084Asn
|
|
ENST00000571763.5:n.405T>A
|
|
|
ENST00000576720.1:n.3438T>A
|
|
|
XM_005255124.3:c.4570T>A
|
XP_005255181.1:p.Tyr1524Asn
|
|
XM_005255124.4:c.4570T>A
|
XP_005255181.1:p.Tyr1524Asn
|
|
XM_005255125.3:c.4198T>A
|
XP_005255182.1:p.Tyr1400Asn
|
|
XM_005255125.4:c.4198T>A
|
XP_005255182.1:p.Tyr1400Asn
|
|
XM_006720848.2:c.4354T>A
|
XP_006720911.1:p.Tyr1452Asn
|
|
XM_006720848.3:c.4354T>A
|
XP_006720911.1:p.Tyr1452Asn
|
|
XM_011522380.1:c.4561T>A
|
XP_011520682.1:p.Tyr1521Asn
|
|
XM_011522381.1:c.3862T>A
|
XP_011520683.1:p.Tyr1288Asn
|
|
XM_011522381.2:c.3862T>A
|
XP_011520683.1:p.Tyr1288Asn
|
|
XM_017022944.1:c.4609T>A
|
XP_016878433.1:p.Tyr1537Asn
|