ENST00000688602.1:c.1394G=
|
|
|
ENST00000689936.1:c.1376G=
|
|
|
ENST00000359596.8:c.12984G=
MANE Select
|
ENSP00000352608.2:p.Ala4328=
|
|
ENST00000355481.8:c.12969G=
|
ENSP00000347667.3:p.Ala4323=
|
|
ENST00000359596.7:c.12984G=
|
ENSP00000352608.2:p.Ala4328=
|
|
ENST00000360985.7:c.12966G=
|
ENSP00000354254.4:p.Ala4322=
|
|
NM_000540.2:c.12984G= , LRG_766t1:c.12984G=
|
NP_000531.2:p.Ala4328=
|
|
NM_001042723.1:c.12969G=
|
NP_001036188.1:p.Ala4323=
|
|
XM_006723317.1:c.12966G=
|
XP_006723380.1:p.Ala4322=
|
|
XM_006723319.1:c.12951G=
|
XP_006723382.1:p.Ala4317=
|
|
XM_011527204.1:c.12981G=
|
XP_011525506.1:p.Ala4327=
|
|
XM_011527205.1:c.12984G=
|
XP_011525507.1:p.Ala4328=
|
|
XM_006723317.2:c.12966G=
|
XP_006723380.1:p.Ala4322=
|
|
XM_006723319.2:c.12951G=
|
XP_006723382.1:p.Ala4317=
|
|
XM_011527205.2:c.12984G=
|
XP_011525507.1:p.Ala4328=
|
|
NM_000540.3:c.12984G=
MANE Select
|
NP_000531.2:p.Ala4328=
|
|
NM_001042723.2:c.12969G=
|
NP_001036188.1:p.Ala4323=
|
|