ENST00000261304.7:c.387C>G
MANE Select
|
ENSP00000261304.2:p.Tyr129Ter
|
|
ENST00000261304.6:c.387C>G
|
ENSP00000261304.2:p.Tyr129Ter
|
|
ENST00000393568.8:c.318C>G
|
ENSP00000377198.4:p.Tyr106Ter
|
|
ENST00000393569.6:c.309C>G
|
ENSP00000377199.2:p.Tyr103Ter
|
|
ENST00000474294.6:n.377C>G
|
|
|
ENST00000544807.6:c.219C>G
|
ENSP00000437513.2:p.Tyr73Ter
|
|
ENST00000554372.5:c.*136C>G
|
ENSP00000451884.1:n.*136C>G
|
|
ENST00000554916.5:n.266C>G
|
|
|
ENST00000556261.5:n.88C>G
|
|
|
ENST00000556879.5:c.447C>G
|
ENSP00000452208.1:n.447C>G
|
|
ENST00000557316.5:c.387C>G
|
ENSP00000452314.1:p.Tyr129Ter
|
|
ENST00000622264.4:c.377C>G
|
|
|
NM_000153.3:c.387C>G
|
NP_000144.2:p.Tyr129Ter
|
|
NM_001201401.1:c.318C>G
|
NP_001188330.1:p.Tyr106Ter
|
|
NM_001201402.1:c.309C>G
|
NP_001188331.1:p.Tyr103Ter
|
|
XM_011536618.1:c.219C>G
|
XP_011534920.1:p.Tyr73Ter
|
|
XM_011536618.2:c.219C>G
|
XP_011534920.1:p.Tyr73Ter
|
|
NM_000153.4:c.387C>G
MANE Select
|
NP_000144.2:p.Tyr129Ter
|
|
NM_001201401.2:c.318C>G
|
NP_001188330.1:p.Tyr106Ter
|
|
NM_001201402.2:c.309C>G
|
NP_001188331.1:p.Tyr103Ter
|
|