ENST00000593677.2:c.903T>A
|
|
|
ENST00000688602.1:c.2300T>A
|
|
|
ENST00000689936.1:c.2272T>A
|
|
|
ENST00000359596.8:c.13967T>A
MANE Select
|
ENSP00000352608.2:p.Phe4656Tyr
|
|
ENST00000355481.8:c.13952T>A
|
ENSP00000347667.3:p.Phe4651Tyr
|
|
ENST00000359596.7:c.13967T>A
|
ENSP00000352608.2:p.Phe4656Tyr
|
|
ENST00000360985.7:c.13949T>A
|
ENSP00000354254.4:p.Phe4650Tyr
|
|
ENST00000593677.1:c.427T>A
|
|
|
NM_000540.2:c.13967T>A , LRG_766t1:c.13967T>A
|
NP_000531.2:p.Phe4656Tyr
|
|
NM_001042723.1:c.13952T>A
|
NP_001036188.1:p.Phe4651Tyr
|
|
XM_006723317.1:c.13949T>A
|
XP_006723380.1:p.Phe4650Tyr
|
|
XM_006723319.1:c.13934T>A
|
XP_006723382.1:p.Phe4645Tyr
|
|
XM_011527204.1:c.13964T>A
|
XP_011525506.1:p.Phe4655Tyr
|
|
XM_011527205.1:c.13880T>A
|
XP_011525507.1:p.Phe4627Tyr
|
|
XM_006723317.2:c.13949T>A
|
XP_006723380.1:p.Phe4650Tyr
|
|
XM_006723319.2:c.13934T>A
|
XP_006723382.1:p.Phe4645Tyr
|
|
XM_011527205.2:c.13880T>A
|
XP_011525507.1:p.Phe4627Tyr
|
|
NM_000540.3:c.13967T>A
MANE Select
|
NP_000531.2:p.Phe4656Tyr
|
|
NM_001042723.2:c.13952T>A
|
NP_001036188.1:p.Phe4651Tyr
|
|