ENST00000593677.2:c.1491A>C
|
|
|
ENST00000688602.1:c.2888A>C
|
|
|
ENST00000689936.1:c.2860A>C
|
|
|
ENST00000359596.8:c.14555A>C
MANE Select
|
ENSP00000352608.2:p.Tyr4852Ser
|
|
ENST00000355481.8:c.14540A>C
|
ENSP00000347667.3:p.Tyr4847Ser
|
|
ENST00000359596.7:c.14555A>C
|
ENSP00000352608.2:p.Tyr4852Ser
|
|
ENST00000360985.7:c.14537A>C
|
ENSP00000354254.4:p.Tyr4846Ser
|
|
NM_000540.2:c.14555A>C , LRG_766t1:c.14555A>C
|
NP_000531.2:p.Tyr4852Ser
|
|
NM_001042723.1:c.14540A>C
|
NP_001036188.1:p.Tyr4847Ser
|
|
XM_006723317.1:c.14537A>C
|
XP_006723380.1:p.Tyr4846Ser
|
|
XM_006723319.1:c.14522A>C
|
XP_006723382.1:p.Tyr4841Ser
|
|
XM_011527204.1:c.14552A>C
|
XP_011525506.1:p.Tyr4851Ser
|
|
XM_011527205.1:c.14468A>C
|
XP_011525507.1:p.Tyr4823Ser
|
|
XM_006723317.2:c.14537A>C
|
XP_006723380.1:p.Tyr4846Ser
|
|
XM_006723319.2:c.14522A>C
|
XP_006723382.1:p.Tyr4841Ser
|
|
XM_011527205.2:c.14468A>C
|
XP_011525507.1:p.Tyr4823Ser
|
|
NM_000540.3:c.14555A>C
MANE Select
|
NP_000531.2:p.Tyr4852Ser
|
|
NM_001042723.2:c.14540A>C
|
NP_001036188.1:p.Tyr4847Ser
|
|