ENST00000593677.2:c.920T>G
|
|
|
ENST00000688602.1:c.2317T>G
|
|
|
ENST00000689936.1:c.2289T>G
|
|
|
ENST00000359596.8:c.13984T>G
MANE Select
|
ENSP00000352608.2:p.Tyr4662Asp
|
|
ENST00000355481.8:c.13969T>G
|
ENSP00000347667.3:p.Tyr4657Asp
|
|
ENST00000359596.7:c.13984T>G
|
ENSP00000352608.2:p.Tyr4662Asp
|
|
ENST00000360985.7:c.13966T>G
|
ENSP00000354254.4:p.Tyr4656Asp
|
|
NM_000540.2:c.13984T>G , LRG_766t1:c.13984T>G
|
NP_000531.2:p.Tyr4662Asp
|
|
NM_001042723.1:c.13969T>G
|
NP_001036188.1:p.Tyr4657Asp
|
|
XM_006723317.1:c.13966T>G
|
XP_006723380.1:p.Tyr4656Asp
|
|
XM_006723319.1:c.13951T>G
|
XP_006723382.1:p.Tyr4651Asp
|
|
XM_011527204.1:c.13981T>G
|
XP_011525506.1:p.Tyr4661Asp
|
|
XM_011527205.1:c.13897T>G
|
XP_011525507.1:p.Tyr4633Asp
|
|
XM_006723317.2:c.13966T>G
|
XP_006723380.1:p.Tyr4656Asp
|
|
XM_006723319.2:c.13951T>G
|
XP_006723382.1:p.Tyr4651Asp
|
|
XM_011527205.2:c.13897T>G
|
XP_011525507.1:p.Tyr4633Asp
|
|
NM_000540.3:c.13984T>G
MANE Select
|
NP_000531.2:p.Tyr4662Asp
|
|
NM_001042723.2:c.13969T>G
|
NP_001036188.1:p.Tyr4657Asp
|
|