ENST00000593677.2:c.1298A>T
|
|
|
ENST00000688602.1:c.2695A>T
|
|
|
ENST00000689936.1:c.2667A>T
|
|
|
ENST00000359596.8:c.14362A>T
MANE Select
|
ENSP00000352608.2:p.Asn4788Tyr
|
|
ENST00000355481.8:c.14347A>T
|
ENSP00000347667.3:p.Asn4783Tyr
|
|
ENST00000359596.7:c.14362A>T
|
ENSP00000352608.2:p.Asn4788Tyr
|
|
ENST00000360985.7:c.14344A>T
|
ENSP00000354254.4:p.Asn4782Tyr
|
|
NM_000540.2:c.14362A>T , LRG_766t1:c.14362A>T
|
NP_000531.2:p.Asn4788Tyr
|
|
NM_001042723.1:c.14347A>T
|
NP_001036188.1:p.Asn4783Tyr
|
|
XM_006723317.1:c.14344A>T
|
XP_006723380.1:p.Asn4782Tyr
|
|
XM_006723319.1:c.14329A>T
|
XP_006723382.1:p.Asn4777Tyr
|
|
XM_011527204.1:c.14359A>T
|
XP_011525506.1:p.Asn4787Tyr
|
|
XM_011527205.1:c.14275A>T
|
XP_011525507.1:p.Asn4759Tyr
|
|
XM_006723317.2:c.14344A>T
|
XP_006723380.1:p.Asn4782Tyr
|
|
XM_006723319.2:c.14329A>T
|
XP_006723382.1:p.Asn4777Tyr
|
|
XM_011527205.2:c.14275A>T
|
XP_011525507.1:p.Asn4759Tyr
|
|
NM_000540.3:c.14362A>T
MANE Select
|
NP_000531.2:p.Asn4788Tyr
|
|
NM_001042723.2:c.14347A>T
|
NP_001036188.1:p.Asn4783Tyr
|
|