ENST00000432588.6:c.387C>A
|
ENSP00000407473.2:p.Thr129=
|
|
ENST00000473257.3:c.258C>A
|
ENSP00000501773.1:p.Thr86=
|
|
ENST00000477812.2:n.934C>A
|
|
|
ENST00000493945.6:c.387C>A
|
ENSP00000494269.1:p.Thr129=
|
|
ENST00000642480.2:c.387C>A
|
ENSP00000495995.2:p.Thr129=
|
|
ENST00000645576.1:c.364-25C>A
|
ENSP00000496101.1:n.364-25C>A
|
|
ENST00000646664.1:c.387C>A
MANE Select
|
ENSP00000494750.1:p.Thr129=
|
|
ENST00000647275.1:c.21C>A
|
ENSP00000494185.1:p.Thr7=
|
|
ENST00000674681.1:c.387C>A
|
ENSP00000502821.1:p.Thr129=
|
|
ENST00000675515.1:c.387C>A
|
ENSP00000501862.1:p.Thr129=
|
|
ENST00000676189.1:c.386C>A
|
ENSP00000502538.1:p.Pro129His
|
|
ENST00000676319.1:c.87+875C>A
|
ENSP00000502193.1:n.87+875C>A
|
|
ENST00000676397.1:c.387C>A
|
ENSP00000502286.1:p.Thr129=
|
|
ENST00000331789.9:c.387C>A
|
ENSP00000349960.4:p.Thr129=
|
|
ENST00000425660.5:c.*50C>A
|
ENSP00000409264.1:n.*50C>A
|
|
ENST00000432588.5:c.387C>A
|
ENSP00000407473.1:p.Thr129=
|
|
ENST00000462494.5:n.912C>A
|
|
|
ENST00000473257.1:n.105C>A
|
|
|
ENST00000477812.1:n.594C>A
|
|
|
ENST00000484841.5:n.542C>A
|
|
|
ENST00000493945.5:n.393C>A
|
|
|
NM_001101.3:c.387C>A , LRG_132t1:c.387C>A
|
NP_001092.1:p.Thr129=
|
|
XM_006715764.1:c.21C>A
|
XP_006715827.1:p.Thr7=
|
|
NM_001101.4:c.387C>A
|
NP_001092.1:p.Thr129=
|
|
NM_001101.5:c.387C>A
MANE Select
|
NP_001092.1:p.Thr129=
|
|