ENST00000593677.2:c.1164G=
|
|
|
ENST00000688602.1:c.2561G=
|
|
|
ENST00000689936.1:c.2533G=
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|
|
ENST00000359596.8:c.14228G=
MANE Select
|
ENSP00000352608.2:p.Gly4743=
|
|
ENST00000355481.8:c.14213G=
|
ENSP00000347667.3:p.Gly4738=
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|
ENST00000359596.7:c.14228G=
|
ENSP00000352608.2:p.Gly4743=
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|
ENST00000360985.7:c.14210G=
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ENSP00000354254.4:p.Gly4737=
|
|
NM_000540.2:c.14228G= , LRG_766t1:c.14228G=
|
NP_000531.2:p.Gly4743=
|
|
NM_001042723.1:c.14213G=
|
NP_001036188.1:p.Gly4738=
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|
XM_006723317.1:c.14210G=
|
XP_006723380.1:p.Gly4737=
|
|
XM_006723319.1:c.14195G=
|
XP_006723382.1:p.Gly4732=
|
|
XM_011527204.1:c.14225G=
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XP_011525506.1:p.Gly4742=
|
|
XM_011527205.1:c.14141G=
|
XP_011525507.1:p.Gly4714=
|
|
XM_006723317.2:c.14210G=
|
XP_006723380.1:p.Gly4737=
|
|
XM_006723319.2:c.14195G=
|
XP_006723382.1:p.Gly4732=
|
|
XM_011527205.2:c.14141G=
|
XP_011525507.1:p.Gly4714=
|
|
NM_000540.3:c.14228G=
MANE Select
|
NP_000531.2:p.Gly4743=
|
|
NM_001042723.2:c.14213G=
|
NP_001036188.1:p.Gly4738=
|
|