ENST00000380044.6:c.466G>T
MANE Select
|
ENSP00000369383.1:p.Ala156Ser
|
|
ENST00000233545.6:c.466G>T
|
ENSP00000233545.2:p.Ala156Ser
|
|
ENST00000357186.10:c.298G>T
|
ENSP00000349713.6:p.Ala100Ser
|
|
ENST00000380044.5:c.466G>T
|
ENSP00000369383.1:p.Ala156Ser
|
|
ENST00000402310.5:c.413G>T
|
ENSP00000383955.1:p.Gly138Val
|
|
ENST00000402722.5:c.*45G>T
|
ENSP00000386000.1:n.*45G>T
|
|
ENST00000405076.5:c.277G>T
|
ENSP00000385175.1:p.Ala93Ser
|
|
ENST00000405983.5:c.511G>T
|
ENSP00000384586.1:p.Ala171Ser
|
|
ENST00000415514.5:c.*267G>T
|
ENSP00000388043.1:n.*267G>T
|
|
ENST00000426513.6:c.*131G>T
|
ENSP00000403824.2:n.*131G>T
|
|
ENST00000430991.5:c.300G>T
|
|
|
ENST00000620797.4:n.139G>T
|
|
|
ENST00000621183.4:n.769G>T
|
|
|
NM_002437.4:c.466G>T
|
NP_002428.1:p.Ala156Ser
|
|
XM_005264326.2:c.466G>T
|
XP_005264383.1:p.Ala156Ser
|
|
XM_005264327.2:c.307G>T
|
XP_005264384.1:p.Ala103Ser
|
|
XM_006712021.2:c.418G>T
|
XP_006712084.1:p.Ala140Ser
|
|
XM_005264326.4:c.466G>T
|
XP_005264383.1:p.Ala156Ser
|
|
XM_006712021.3:c.418G>T
|
XP_006712084.1:p.Ala140Ser
|
|
XM_017004150.1:c.448G>T
|
XP_016859639.1:p.Ala150Ser
|
|
XM_017004151.1:c.418G>T
|
XP_016859640.1:p.Ala140Ser
|
|
XM_017004152.1:c.307G>T
|
XP_016859641.1:p.Ala103Ser
|
|
XM_024452913.1:c.418G>T
|
XP_024308681.1:p.Ala140Ser
|
|
NM_002437.5:c.466G>T
MANE Select
|
NP_002428.1:p.Ala156Ser
|
|