ENST00000594045.2:c.*389G>A
|
ENSP00000472329.2:n.*389G>A
|
|
ENST00000594442.2:c.424G>A
|
ENSP00000471239.2:p.Ala142Thr
|
|
ENST00000597629.3:c.406G>A
MANE Select
|
ENSP00000469647.2:p.Ala136Thr
|
|
ENST00000652583.1:n.455G>A
|
|
|
ENST00000594045.1:c.*389G>A
|
ENSP00000472329.1:n.*389G>A
|
|
ENST00000594442.1:c.455G>A
|
|
|
ENST00000597629.1:c.424G>A
|
ENSP00000469647.1:p.Ala142Thr
|
|
ENST00000600033.1:c.425G>A
|
|
|
NM_003407.3:c.424G>A
|
NP_003398.2:p.Ala142Thr
|
|
NM_003407.4:c.406G>A
|
NP_003398.3:p.Ala136Thr
|
|
NM_003407.5:c.406G>A
MANE Select
|
NP_003398.3:p.Ala136Thr
|
|