ENST00000456935.7:c.1462G>T
MANE Select
|
ENSP00000395473.2:p.Asp488Tyr
|
|
ENST00000221363.8:c.1459G>T
|
ENSP00000221363.4:p.Asp487Tyr
|
|
ENST00000433513.5:n.68G>T
|
|
|
ENST00000456935.6:c.1462G>T
|
ENSP00000395473.2:p.Asp488Tyr
|
|
ENST00000466794.5:n.1361G>T
|
|
|
ENST00000495617.1:n.638G>T
|
|
|
ENST00000593686.1:c.72G>T
|
|
|
ENST00000595880.5:n.59G>T
|
|
|
NM_000528.3:c.1462G>T
|
NP_000519.2:p.Asp488Tyr
|
|
NM_001173498.1:c.1459G>T
|
NP_001166969.1:p.Asp487Tyr
|
|
XM_005259913.1:c.1465G>T
|
XP_005259970.1:p.Asp489Tyr
|
|
XM_011528017.1:c.361G>T
|
XP_011526319.1:p.Asp121Tyr
|
|
XM_005259913.2:c.1465G>T
|
XP_005259970.1:p.Asp489Tyr
|
|
XM_024451518.1:c.361G>T
|
XP_024307286.1:p.Asp121Tyr
|
|
NM_000528.4:c.1462G>T
MANE Select
|
NP_000519.2:p.Asp488Tyr
|
|
NM_001173498.2:c.1459G>T
|
NP_001166969.1:p.Asp487Tyr
|
|