ENST00000558767.6:c.244A>T
|
ENSP00000507680.1:p.Arg82Ter
|
|
ENST00000682012.1:n.319A>T
|
|
|
ENST00000683593.1:n.121A>T
|
|
|
ENST00000684363.1:c.244A>T
|
ENSP00000507314.1:p.Arg82Ter
|
|
ENST00000684569.1:n.289A>T
|
|
|
ENST00000561421.6:c.244A>T
MANE Select
|
ENSP00000453347.2:p.Arg82Ter
|
|
ENST00000646551.1:n.1731A>T
|
|
|
ENST00000261755.9:c.244A>T
|
ENSP00000261755.5:p.Arg82Ter
|
|
ENST00000407106.5:c.244A>T
|
ENSP00000385080.1:p.Arg82Ter
|
|
ENST00000537726.5:n.326A>T
|
|
|
ENST00000539156.5:c.34A>T
|
ENSP00000454271.1:p.Arg12Ter
|
|
ENST00000558022.5:c.244A>T
|
ENSP00000453152.1:p.Arg82Ter
|
|
ENST00000558767.5:n.505A>T
|
|
|
ENST00000561369.1:n.324A>T
|
|
|
ENST00000561421.5:c.244A>T
|
ENSP00000453347.1:p.Arg82Ter
|
|
NM_000137.2:c.244A>T
|
NP_000128.1:p.Arg82Ter
|
|
XM_024449872.1:c.244A>T
|
XP_024305640.1:p.Arg82Ter
|
|
NM_000137.4:c.244A>T
MANE Select
|
NP_000128.1:p.Arg82Ter
|
|
NM_001374377.1:c.244A>T
|
NP_001361306.1:p.Arg82Ter
|
|
NM_001374380.1:c.244A>T
|
NP_001361309.1:p.Arg82Ter
|
|