|
NM_032119.4:c.13017T>A
MANE Select
|
NP_115495.3:p.Asp4339Glu
|
|
ENST00000405460.9:c.13017T>A
MANE Select
|
ENSP00000384582.2:p.Asp4339Glu
|
|
NM_032119.3:c.13017T>A
|
NP_115495.3:p.Asp4339Glu
|
|
NR_003149.1:n.13030T>A
|
|
|
NR_003149.2:n.13033T>A
|
|
|
ENST00000405460.6:c.13017T>A
|
ENSP00000384582.2:p.Asp4339Glu
|
|
ENST00000425867.3:c.1971T>A
|
ENSP00000392618.3:p.Asp657Glu
|
|
ENST00000639431.1:c.265+102823T>A
|
ENSP00000491057.1:n.265+102823T>A
|
|
ENST00000640464.1:n.3436T>A
|
|
|
XM_011543675.1:c.13014T>A
|
XP_011541977.1:p.Asp4338Glu
|
|
XM_011543676.1:c.12936T>A
|
XP_011541978.1:p.Asp4312Glu
|
|
XM_011543677.1:c.10320T>A
|
XP_011541979.1:p.Asp3440Glu
|
|
XM_011543678.1:c.13017T>A
|
XP_011541980.1:p.Asp4339Glu
|
|
XM_017009963.2:c.13038T>A
|
XP_016865452.1:p.Asp4346Glu
|
|
XM_017009964.2:c.13035T>A
|
XP_016865453.1:p.Asp4345Glu
|
|
XM_017009965.1:c.13035T>A
|
XP_016865454.1:p.Asp4345Glu
|
|
XM_017009966.2:c.12957T>A
|
XP_016865455.1:p.Asp4319Glu
|
|
XM_017009967.1:c.12942T>A
|
XP_016865456.1:p.Asp4314Glu
|
|
XM_017009968.2:c.13038T>A
|
XP_016865457.1:p.Asp4346Glu
|
|
XM_017009969.2:c.13038T>A
|
XP_016865458.1:p.Asp4346Glu
|
|
XM_017009970.2:c.13038T>A
|
XP_016865459.1:p.Asp4346Glu
|
|
XM_017009971.2:c.13038T>A
|
XP_016865460.1:p.Asp4346Glu
|
|
XM_017009972.1:c.6156T>A
|
XP_016865461.1:p.Asp2052Glu
|
|
XM_017009973.1:c.6135T>A
|
XP_016865462.1:p.Asp2045Glu
|