ENST00000261304.7:c.454T>G
MANE Select
|
ENSP00000261304.2:p.Ser152Ala
|
|
ENST00000261304.6:c.454T>G
|
ENSP00000261304.2:p.Ser152Ala
|
|
ENST00000393568.8:c.385T>G
|
ENSP00000377198.4:p.Ser129Ala
|
|
ENST00000393569.6:c.376T>G
|
ENSP00000377199.2:p.Ser126Ala
|
|
ENST00000474294.6:n.444T>G
|
|
|
ENST00000544807.6:c.286T>G
|
ENSP00000437513.2:p.Ser96Ala
|
|
ENST00000554372.5:c.*203T>G
|
ENSP00000451884.1:n.*203T>G
|
|
ENST00000554916.5:n.333T>G
|
|
|
ENST00000556261.5:n.155T>G
|
|
|
ENST00000556879.5:c.514T>G
|
ENSP00000452208.1:n.514T>G
|
|
ENST00000557316.5:c.454T>G
|
ENSP00000452314.1:p.Ser152Ala
|
|
ENST00000622264.4:c.444T>G
|
|
|
NM_000153.3:c.454T>G
|
NP_000144.2:p.Ser152Ala
|
|
NM_001201401.1:c.385T>G
|
NP_001188330.1:p.Ser129Ala
|
|
NM_001201402.1:c.376T>G
|
NP_001188331.1:p.Ser126Ala
|
|
XM_011536618.1:c.286T>G
|
XP_011534920.1:p.Ser96Ala
|
|
XM_011536618.2:c.286T>G
|
XP_011534920.1:p.Ser96Ala
|
|
NM_000153.4:c.454T>G
MANE Select
|
NP_000144.2:p.Ser152Ala
|
|
NM_001201401.2:c.385T>G
|
NP_001188330.1:p.Ser129Ala
|
|
NM_001201402.2:c.376T>G
|
NP_001188331.1:p.Ser126Ala
|
|