ENST00000470094.2:c.775A>T
|
ENSP00000434898.2:p.Arg259Ter
|
|
ENST00000528762.2:c.775A>T
|
ENSP00000433168.2:p.Arg259Ter
|
|
ENST00000530893.7:c.406A>T
|
ENSP00000499438.2:p.Arg136Ter
|
|
ENST00000665585.2:c.775A>T
|
ENSP00000499570.2:p.Arg259Ter
|
|
ENST00000666593.2:c.775A>T
|
ENSP00000499256.2:p.Arg259Ter
|
|
ENST00000700202.2:c.775A>T
|
ENSP00000514856.2:p.Arg259Ter
|
|
ENST00000700201.1:c.*554A>T
|
ENSP00000514855.1:n.*554A>T
|
|
ENST00000380152.8:c.775A>T
MANE Select
|
ENSP00000369497.3:p.Arg259Ter
|
|
ENST00000544455.6:c.775A>T
|
ENSP00000439902.1:p.Arg259Ter
|
|
ENST00000614259.2:c.775A>T
|
ENSP00000506251.1:p.Arg259Ter
|
|
ENST00000680887.1:c.775A>T
|
ENSP00000505508.1:p.Arg259Ter
|
|
ENST00000380152.7:c.775A>T
|
ENSP00000369497.3:p.Arg259Ter
|
|
ENST00000530893.6:n.973A>T
|
|
|
ENST00000544455.5:c.775A>T
|
ENSP00000439902.1:p.Arg259Ter
|
|
ENST00000614259.1:n.775A>T
|
|
|
NM_000059.3:c.775A>T , LRG_293t1:c.775A>T
|
NP_000050.2:p.Arg259Ter
|
|
XM_011535203.1:c.775A>T
|
XP_011533505.1:p.Arg259Ter
|
|
XM_011535204.1:c.775A>T
|
XP_011533506.1:p.Arg259Ter
|
|
XM_011535205.1:c.775A>T
|
XP_011533507.1:p.Arg259Ter
|
|
NM_000059.4:c.775A>T
MANE Select
|
NP_000050.3:p.Arg259Ter
|
|