ENST00000593677.2:c.887C>A
|
|
|
ENST00000688602.1:c.2284C>A
|
|
|
ENST00000689936.1:c.2256C>A
|
|
|
ENST00000359596.8:c.13951C>A
MANE Select
|
ENSP00000352608.2:p.His4651Asn
|
|
ENST00000355481.8:c.13936C>A
|
ENSP00000347667.3:p.His4646Asn
|
|
ENST00000359596.7:c.13951C>A
|
ENSP00000352608.2:p.His4651Asn
|
|
ENST00000360985.7:c.13933C>A
|
ENSP00000354254.4:p.His4645Asn
|
|
ENST00000593677.1:c.411C>A
|
|
|
NM_000540.2:c.13951C>A , LRG_766t1:c.13951C>A
|
NP_000531.2:p.His4651Asn
|
|
NM_001042723.1:c.13936C>A
|
NP_001036188.1:p.His4646Asn
|
|
XM_006723317.1:c.13933C>A
|
XP_006723380.1:p.His4645Asn
|
|
XM_006723319.1:c.13918C>A
|
XP_006723382.1:p.His4640Asn
|
|
XM_011527204.1:c.13948C>A
|
XP_011525506.1:p.His4650Asn
|
|
XM_011527205.1:c.13864C>A
|
XP_011525507.1:p.His4622Asn
|
|
XM_006723317.2:c.13933C>A
|
XP_006723380.1:p.His4645Asn
|
|
XM_006723319.2:c.13918C>A
|
XP_006723382.1:p.His4640Asn
|
|
XM_011527205.2:c.13864C>A
|
XP_011525507.1:p.His4622Asn
|
|
NM_000540.3:c.13951C>A
MANE Select
|
NP_000531.2:p.His4651Asn
|
|
NM_001042723.2:c.13936C>A
|
NP_001036188.1:p.His4646Asn
|
|