ENST00000593677.2:c.1289T>A
|
|
|
ENST00000688602.1:c.2686T>A
|
|
|
ENST00000689936.1:c.2658T>A
|
|
|
ENST00000359596.8:c.14353T>A
MANE Select
|
ENSP00000352608.2:p.Phe4785Ile
|
|
ENST00000355481.8:c.14338T>A
|
ENSP00000347667.3:p.Phe4780Ile
|
|
ENST00000359596.7:c.14353T>A
|
ENSP00000352608.2:p.Phe4785Ile
|
|
ENST00000360985.7:c.14335T>A
|
ENSP00000354254.4:p.Phe4779Ile
|
|
NM_000540.2:c.14353T>A , LRG_766t1:c.14353T>A
|
NP_000531.2:p.Phe4785Ile
|
|
NM_001042723.1:c.14338T>A
|
NP_001036188.1:p.Phe4780Ile
|
|
XM_006723317.1:c.14335T>A
|
XP_006723380.1:p.Phe4779Ile
|
|
XM_006723319.1:c.14320T>A
|
XP_006723382.1:p.Phe4774Ile
|
|
XM_011527204.1:c.14350T>A
|
XP_011525506.1:p.Phe4784Ile
|
|
XM_011527205.1:c.14266T>A
|
XP_011525507.1:p.Phe4756Ile
|
|
XM_006723317.2:c.14335T>A
|
XP_006723380.1:p.Phe4779Ile
|
|
XM_006723319.2:c.14320T>A
|
XP_006723382.1:p.Phe4774Ile
|
|
XM_011527205.2:c.14266T>A
|
XP_011525507.1:p.Phe4756Ile
|
|
NM_000540.3:c.14353T>A
MANE Select
|
NP_000531.2:p.Phe4785Ile
|
|
NM_001042723.2:c.14338T>A
|
NP_001036188.1:p.Phe4780Ile
|
|