ENST00000593677.2:c.1524T>A
|
|
|
ENST00000688602.1:c.2921T>A
|
|
|
ENST00000689936.1:c.2893T>A
|
|
|
ENST00000359596.8:c.14588T>A
MANE Select
|
ENSP00000352608.2:p.Phe4863Tyr
|
|
ENST00000355481.8:c.14573T>A
|
ENSP00000347667.3:p.Phe4858Tyr
|
|
ENST00000359596.7:c.14588T>A
|
ENSP00000352608.2:p.Phe4863Tyr
|
|
ENST00000360985.7:c.14570T>A
|
ENSP00000354254.4:p.Phe4857Tyr
|
|
NM_000540.2:c.14588T>A , LRG_766t1:c.14588T>A
|
NP_000531.2:p.Phe4863Tyr
|
|
NM_001042723.1:c.14573T>A
|
NP_001036188.1:p.Phe4858Tyr
|
|
XM_006723317.1:c.14570T>A
|
XP_006723380.1:p.Phe4857Tyr
|
|
XM_006723319.1:c.14555T>A
|
XP_006723382.1:p.Phe4852Tyr
|
|
XM_011527204.1:c.14585T>A
|
XP_011525506.1:p.Phe4862Tyr
|
|
XM_011527205.1:c.14501T>A
|
XP_011525507.1:p.Phe4834Tyr
|
|
XM_006723317.2:c.14570T>A
|
XP_006723380.1:p.Phe4857Tyr
|
|
XM_006723319.2:c.14555T>A
|
XP_006723382.1:p.Phe4852Tyr
|
|
XM_011527205.2:c.14501T>A
|
XP_011525507.1:p.Phe4834Tyr
|
|
NM_000540.3:c.14588T>A
MANE Select
|
NP_000531.2:p.Phe4863Tyr
|
|
NM_001042723.2:c.14573T>A
|
NP_001036188.1:p.Phe4858Tyr
|
|