ENST00000593677.2:c.1262T>A
|
|
|
ENST00000688602.1:c.2659T>A
|
|
|
ENST00000689936.1:c.2631T>A
|
|
|
ENST00000359596.8:c.14326T>A
MANE Select
|
ENSP00000352608.2:p.Tyr4776Asn
|
|
ENST00000355481.8:c.14311T>A
|
ENSP00000347667.3:p.Tyr4771Asn
|
|
ENST00000359596.7:c.14326T>A
|
ENSP00000352608.2:p.Tyr4776Asn
|
|
ENST00000360985.7:c.14308T>A
|
ENSP00000354254.4:p.Tyr4770Asn
|
|
NM_000540.2:c.14326T>A , LRG_766t1:c.14326T>A
|
NP_000531.2:p.Tyr4776Asn
|
|
NM_001042723.1:c.14311T>A
|
NP_001036188.1:p.Tyr4771Asn
|
|
XM_006723317.1:c.14308T>A
|
XP_006723380.1:p.Tyr4770Asn
|
|
XM_006723319.1:c.14293T>A
|
XP_006723382.1:p.Tyr4765Asn
|
|
XM_011527204.1:c.14323T>A
|
XP_011525506.1:p.Tyr4775Asn
|
|
XM_011527205.1:c.14239T>A
|
XP_011525507.1:p.Tyr4747Asn
|
|
XM_006723317.2:c.14308T>A
|
XP_006723380.1:p.Tyr4770Asn
|
|
XM_006723319.2:c.14293T>A
|
XP_006723382.1:p.Tyr4765Asn
|
|
XM_011527205.2:c.14239T>A
|
XP_011525507.1:p.Tyr4747Asn
|
|
NM_000540.3:c.14326T>A
MANE Select
|
NP_000531.2:p.Tyr4776Asn
|
|
NM_001042723.2:c.14311T>A
|
NP_001036188.1:p.Tyr4771Asn
|
|