ENST00000262093.11:c.1249T>G
MANE Select
|
ENSP00000262093.6:p.Phe417Val
|
|
ENST00000382873.8:c.1033T>G
|
ENSP00000372326.4:p.Phe345Val
|
|
ENST00000651787.1:n.1355T>G
|
|
|
ENST00000652755.1:c.1267T>G
|
ENSP00000498358.1:p.Phe423Val
|
|
ENST00000262093.9:c.1249T>G
|
ENSP00000262093.5:p.Phe417Val
|
|
ENST00000382873.7:c.1267T>G
|
ENSP00000372326.3:p.Phe423Val
|
|
ENST00000585494.5:c.*976T>G
|
ENSP00000465243.1:n.*976T>G
|
|
NM_000140.3:c.1249T>G
|
NP_000131.2:p.Phe417Val
|
|
NM_001012515.2:c.1267T>G
|
NP_001012533.1:p.Phe423Val
|
|
XM_011525881.1:c.1168T>G
|
XP_011524183.1:p.Phe390Val
|
|
XM_011525882.1:c.1033T>G
|
XP_011524184.1:p.Phe345Val
|
|
NM_000140.4:c.1249T>G
|
NP_000131.2:p.Phe417Val
|
|
NM_001012515.3:c.1267T>G
|
NP_001012533.1:p.Phe423Val
|
|
XM_011525882.2:c.1033T>G
|
XP_011524184.1:p.Phe345Val
|
|
XM_017025614.2:c.1150T>G
|
XP_016881103.1:p.Phe384Val
|
|
NM_000140.5:c.1249T>G
MANE Select
|
NP_000131.2:p.Phe417Val
|
|
NM_001012515.4:c.1267T>G
|
NP_001012533.1:p.Phe423Val
|
|
NM_001371094.1:c.1150T>G
|
NP_001358023.1:p.Phe384Val
|
|
NM_001371095.1:c.1033T>G
|
NP_001358024.1:p.Phe345Val
|
|
NM_001374778.1:c.1189T>G
|
NP_001361707.1:p.Phe397Val
|
|