ENST00000498907.3:c.389G>T
MANE Select
|
ENSP00000427514.1:p.Gly130Val
|
|
ENST00000498907.2:c.389G>T
|
ENSP00000427514.1:p.Gly130Val
|
|
NM_001285829.1:c.32G>T
|
NP_001272758.1:p.Gly11Val
|
|
NM_001287424.1:c.494G>T
|
NP_001274353.1:p.Gly165Val
|
|
NM_001287435.1:c.347G>T
|
NP_001274364.1:p.Gly116Val
|
|
NM_004364.4:c.389G>T
|
NP_004355.2:p.Gly130Val
|
|
NM_001287424.2:c.494G>T
|
NP_001274353.1:p.Gly165Val
|
|
NM_004364.5:c.389G>T
MANE Select
|
NP_004355.2:p.Gly130Val
|
|
NM_001285829.2:c.32G>T
|
NP_001272758.1:p.Gly11Val
|
|
NM_001287435.2:c.347G>T
|
NP_001274364.1:p.Gly116Val
|
|