ENST00000593677.2:c.920T>A
|
|
|
ENST00000688602.1:c.2317T>A
|
|
|
ENST00000689936.1:c.2289T>A
|
|
|
ENST00000359596.8:c.13984T>A
MANE Select
|
ENSP00000352608.2:p.Tyr4662Asn
|
|
ENST00000355481.8:c.13969T>A
|
ENSP00000347667.3:p.Tyr4657Asn
|
|
ENST00000359596.7:c.13984T>A
|
ENSP00000352608.2:p.Tyr4662Asn
|
|
ENST00000360985.7:c.13966T>A
|
ENSP00000354254.4:p.Tyr4656Asn
|
|
NM_000540.2:c.13984T>A , LRG_766t1:c.13984T>A
|
NP_000531.2:p.Tyr4662Asn
|
|
NM_001042723.1:c.13969T>A
|
NP_001036188.1:p.Tyr4657Asn
|
|
XM_006723317.1:c.13966T>A
|
XP_006723380.1:p.Tyr4656Asn
|
|
XM_006723319.1:c.13951T>A
|
XP_006723382.1:p.Tyr4651Asn
|
|
XM_011527204.1:c.13981T>A
|
XP_011525506.1:p.Tyr4661Asn
|
|
XM_011527205.1:c.13897T>A
|
XP_011525507.1:p.Tyr4633Asn
|
|
XM_006723317.2:c.13966T>A
|
XP_006723380.1:p.Tyr4656Asn
|
|
XM_006723319.2:c.13951T>A
|
XP_006723382.1:p.Tyr4651Asn
|
|
XM_011527205.2:c.13897T>A
|
XP_011525507.1:p.Tyr4633Asn
|
|
NM_000540.3:c.13984T>A
MANE Select
|
NP_000531.2:p.Tyr4662Asn
|
|
NM_001042723.2:c.13969T>A
|
NP_001036188.1:p.Tyr4657Asn
|
|