ENST00000593677.2:c.1168G>A
|
|
|
ENST00000688602.1:c.2565G>A
|
|
|
ENST00000689936.1:c.2537G>A
|
|
|
ENST00000359596.8:c.14232G>A
MANE Select
|
ENSP00000352608.2:p.Met4744Ile
|
|
ENST00000355481.8:c.14217G>A
|
ENSP00000347667.3:p.Met4739Ile
|
|
ENST00000359596.7:c.14232G>A
|
ENSP00000352608.2:p.Met4744Ile
|
|
ENST00000360985.7:c.14214G>A
|
ENSP00000354254.4:p.Met4738Ile
|
|
NM_000540.2:c.14232G>A , LRG_766t1:c.14232G>A
|
NP_000531.2:p.Met4744Ile
|
|
NM_001042723.1:c.14217G>A
|
NP_001036188.1:p.Met4739Ile
|
|
XM_006723317.1:c.14214G>A
|
XP_006723380.1:p.Met4738Ile
|
|
XM_006723319.1:c.14199G>A
|
XP_006723382.1:p.Met4733Ile
|
|
XM_011527204.1:c.14229G>A
|
XP_011525506.1:p.Met4743Ile
|
|
XM_011527205.1:c.14145G>A
|
XP_011525507.1:p.Met4715Ile
|
|
XM_006723317.2:c.14214G>A
|
XP_006723380.1:p.Met4738Ile
|
|
XM_006723319.2:c.14199G>A
|
XP_006723382.1:p.Met4733Ile
|
|
XM_011527205.2:c.14145G>A
|
XP_011525507.1:p.Met4715Ile
|
|
NM_000540.3:c.14232G>A
MANE Select
|
NP_000531.2:p.Met4744Ile
|
|
NM_001042723.2:c.14217G>A
|
NP_001036188.1:p.Met4739Ile
|
|