ENST00000438257.9:c.386G>T
MANE Select
|
ENSP00000405854.5:p.Gly129Val
|
|
ENST00000555750.2:c.*224G>T
|
ENSP00000450980.2:n.*224G>T
|
|
ENST00000422005.7:c.*187G>T
|
ENSP00000411438.4:n.*187G>T
|
|
ENST00000438257.8:c.386G>T
|
ENSP00000405854.4:p.Gly129Val
|
|
ENST00000555750.1:c.494G>T
|
ENSP00000450980.1:p.Gly165Val
|
|
ENST00000555844.1:c.470G>T
|
|
|
ENST00000556811.5:c.362G>T
|
|
|
ENST00000557010.5:c.386G>T
|
ENSP00000451419.1:p.Gly129Val
|
|
ENST00000557125.1:c.49-39G>T
|
ENSP00000450547.1:n.49-39G>T
|
|
NM_000793.5:c.386G>T
|
NP_000784.2:p.Gly129Val
|
|
NM_001007023.3:c.494G>T
|
NP_001007024.1:p.Gly165Val
|
|
NM_001242502.1:c.*187G>T
|
NP_001229431.1:n.*187G>T
|
|
NM_001242503.1:c.*187G>T
|
NP_001229432.1:n.*187G>T
|
|
NM_013989.4:c.386G>T
|
NP_054644.1:p.Gly129Val
|
|
NM_000793.6:c.386G>T
|
NP_000784.3:p.Gly129Val
|
|
NM_001324462.2:c.386G>T
|
NP_001311391.2:p.Gly129Val
|
|
NM_001366496.1:c.386G>T
|
NP_001353425.1:p.Gly129Val
|
|
NM_013989.5:c.386G>T
MANE Select
|
NP_054644.1:p.Gly129Val
|
|
NR_158990.1:n.526G>T
|
|
|
NR_158991.1:n.660G>T
|
|
|