ENST00000288723.9:c.409C>T
MANE Plus Clinical
|
ENSP00000288723.4:p.Arg137Ter
|
|
ENST00000330852.10:c.409C>T
MANE Select
|
ENSP00000328551.5:p.Arg137Ter
|
|
ENST00000288723.8:c.409C>T
|
ENSP00000288723.4:p.Arg137Ter
|
|
ENST00000330852.9:c.409C>T
|
ENSP00000328551.5:p.Arg137Ter
|
|
ENST00000338176.8:c.409C>T
|
ENSP00000340079.4:p.Arg137Ter
|
|
ENST00000504644.1:c.18C>T
|
|
|
ENST00000508274.5:c.279C>T
|
ENSP00000424043.1:p.Cys93=
|
|
ENST00000511649.5:c.176C>T
|
|
|
ENST00000630951.1:c.279C>T
|
ENSP00000485808.1:p.Cys93=
|
|
NM_001017979.2:c.409C>T
|
NP_001017979.1:p.Arg137Ter
|
|
NM_001159601.1:c.409C>T
|
NP_001153073.1:p.Arg137Ter
|
|
NM_004249.3:c.409C>T
|
NP_004240.2:p.Arg137Ter
|
|
XM_005248215.3:c.409C>T
|
XP_005248272.1:p.Arg137Ter
|
|
XM_011513911.1:c.409C>T
|
XP_011512213.1:p.Arg137Ter
|
|
XM_011513912.1:c.178C>T
|
XP_011512214.1:p.Arg60Ter
|
|
XR_925360.1:n.624C>T
|
|
|
XR_925361.1:n.624C>T
|
|
|
XR_925363.1:n.742C>T
|
|
|
NM_001017979.3:c.409C>T
MANE Select
|
NP_001017979.1:p.Arg137Ter
|
|
NM_004249.4:c.409C>T
MANE Plus Clinical
|
NP_004240.2:p.Arg137Ter
|
|
NM_001159601.2:c.409C>T
|
NP_001153073.1:p.Arg137Ter
|
|