ENST00000218099.7:c.506C>A
MANE Select
|
ENSP00000218099.2:p.Ser169Tyr
|
|
ENST00000643157.1:n.1173C>A
|
|
|
ENST00000218099.6:c.506C>A
|
ENSP00000218099.2:p.Ser169Tyr
|
|
ENST00000394090.2:c.392C>A
|
ENSP00000377650.2:p.Ser131Tyr
|
|
NM_000133.3:c.506C>A , LRG_556t1:c.506C>A
|
NP_000124.1:p.Ser169Tyr
|
|
NM_001313913.1:c.392C>A
|
NP_001300842.1:p.Ser131Tyr
|
|
XM_005262397.3:c.392-2585C>A
|
XP_005262454.1:n.392-2585C>A
|
|
XM_005262397.4:c.392-2585C>A
|
XP_005262454.1:n.392-2585C>A
|
|
NM_000133.4:c.506C>A
MANE Select
|
NP_000124.1:p.Ser169Tyr
|
|
NM_001313913.2:c.392C>A
|
NP_001300842.1:p.Ser131Tyr
|
|