ENST00000380044.6:c.465G>T
MANE Select
|
ENSP00000369383.1:p.Leu155Phe
|
|
ENST00000233545.6:c.465G>T
|
ENSP00000233545.2:p.Leu155Phe
|
|
ENST00000357186.10:c.297G>T
|
ENSP00000349713.6:p.Leu99Phe
|
|
ENST00000380044.5:c.465G>T
|
ENSP00000369383.1:p.Leu155Phe
|
|
ENST00000402310.5:c.412G>T
|
ENSP00000383955.1:p.Gly138Cys
|
|
ENST00000402722.5:c.*44G>T
|
ENSP00000386000.1:n.*44G>T
|
|
ENST00000405076.5:c.276G>T
|
ENSP00000385175.1:p.Leu92Phe
|
|
ENST00000405983.5:c.510G>T
|
ENSP00000384586.1:p.Leu170Phe
|
|
ENST00000415514.5:c.*266G>T
|
ENSP00000388043.1:n.*266G>T
|
|
ENST00000426513.6:c.*130G>T
|
ENSP00000403824.2:n.*130G>T
|
|
ENST00000430991.5:c.299G>T
|
|
|
ENST00000620797.4:n.138G>T
|
|
|
ENST00000621183.4:n.768G>T
|
|
|
NM_002437.4:c.465G>T
|
NP_002428.1:p.Leu155Phe
|
|
XM_005264326.2:c.465G>T
|
XP_005264383.1:p.Leu155Phe
|
|
XM_005264327.2:c.306G>T
|
XP_005264384.1:p.Leu102Phe
|
|
XM_006712021.2:c.417G>T
|
XP_006712084.1:p.Leu139Phe
|
|
XM_005264326.4:c.465G>T
|
XP_005264383.1:p.Leu155Phe
|
|
XM_006712021.3:c.417G>T
|
XP_006712084.1:p.Leu139Phe
|
|
XM_017004150.1:c.447G>T
|
XP_016859639.1:p.Leu149Phe
|
|
XM_017004151.1:c.417G>T
|
XP_016859640.1:p.Leu139Phe
|
|
XM_017004152.1:c.306G>T
|
XP_016859641.1:p.Leu102Phe
|
|
XM_024452913.1:c.417G>T
|
XP_024308681.1:p.Leu139Phe
|
|
NM_002437.5:c.465G>T
MANE Select
|
NP_002428.1:p.Leu155Phe
|
|