ENST00000261304.7:c.357T>A
MANE Select
|
ENSP00000261304.2:p.Tyr119Ter
|
|
ENST00000261304.6:c.357T>A
|
ENSP00000261304.2:p.Tyr119Ter
|
|
ENST00000393568.8:c.288T>A
|
ENSP00000377198.4:p.Tyr96Ter
|
|
ENST00000393569.6:c.279T>A
|
ENSP00000377199.2:p.Tyr93Ter
|
|
ENST00000474294.6:n.347T>A
|
|
|
ENST00000544807.6:c.189T>A
|
ENSP00000437513.2:p.Tyr63Ter
|
|
ENST00000554372.5:c.*106T>A
|
ENSP00000451884.1:n.*106T>A
|
|
ENST00000554916.5:n.236T>A
|
|
|
ENST00000556261.5:n.58T>A
|
|
|
ENST00000556879.5:c.417T>A
|
ENSP00000452208.1:n.417T>A
|
|
ENST00000557316.5:c.357T>A
|
ENSP00000452314.1:p.Tyr119Ter
|
|
ENST00000622264.4:c.347T>A
|
|
|
NM_000153.3:c.357T>A
|
NP_000144.2:p.Tyr119Ter
|
|
NM_001201401.1:c.288T>A
|
NP_001188330.1:p.Tyr96Ter
|
|
NM_001201402.1:c.279T>A
|
NP_001188331.1:p.Tyr93Ter
|
|
XM_011536618.1:c.189T>A
|
XP_011534920.1:p.Tyr63Ter
|
|
XM_011536618.2:c.189T>A
|
XP_011534920.1:p.Tyr63Ter
|
|
NM_000153.4:c.357T>A
MANE Select
|
NP_000144.2:p.Tyr119Ter
|
|
NM_001201401.2:c.288T>A
|
NP_001188330.1:p.Tyr96Ter
|
|
NM_001201402.2:c.279T>A
|
NP_001188331.1:p.Tyr93Ter
|
|