ENST00000218099.7:c.865C>T
MANE Select
|
ENSP00000218099.2:p.His289Tyr
|
|
ENST00000643157.1:n.1532C>T
|
|
|
ENST00000218099.6:c.865C>T
|
ENSP00000218099.2:p.His289Tyr
|
|
ENST00000394090.2:c.751C>T
|
ENSP00000377650.2:p.His251Tyr
|
|
NM_000133.3:c.865C>T , LRG_556t1:c.865C>T
|
NP_000124.1:p.His289Tyr
|
|
NM_001313913.1:c.751C>T
|
NP_001300842.1:p.His251Tyr
|
|
XM_005262397.3:c.736C>T
|
XP_005262454.1:p.His246Tyr
|
|
XM_005262397.4:c.736C>T
|
XP_005262454.1:p.His246Tyr
|
|
NM_000133.4:c.865C>T
MANE Select
|
NP_000124.1:p.His289Tyr
|
|
NM_001313913.2:c.751C>T
|
NP_001300842.1:p.His251Tyr
|
|