ENST00000405460.9:c.16266T>G
MANE Select
|
ENSP00000384582.2:p.Asp5422Glu
|
|
ENST00000425867.3:c.5220T>G
|
ENSP00000392618.3:p.Asp1740Glu
|
|
ENST00000638510.1:n.3533T>G
|
|
|
ENST00000639431.1:c.265+147285T>G
|
ENSP00000491057.1:n.265+147285T>G
|
|
ENST00000640061.1:n.128+1312T>G
|
|
|
ENST00000640407.1:c.2676T>G
|
ENSP00000491425.1:p.Asp892Glu
|
|
ENST00000405460.6:c.16266T>G
|
ENSP00000384582.2:p.Asp5422Glu
|
|
ENST00000425867.2:c.3249T>G
|
ENSP00000392618.2:p.Asp1083Glu
|
|
NM_032119.3:c.16266T>G
|
NP_115495.3:p.Asp5422Glu
|
|
NR_003149.1:n.16279T>G
|
|
|
XM_011543675.1:c.16263T>G
|
XP_011541977.1:p.Asp5421Glu
|
|
XM_011543676.1:c.16185T>G
|
XP_011541978.1:p.Asp5395Glu
|
|
XM_011543677.1:c.13569T>G
|
XP_011541979.1:p.Asp4523Glu
|
|
NM_032119.4:c.16266T>G
MANE Select
|
NP_115495.3:p.Asp5422Glu
|
|
XM_017009963.2:c.16287T>G
|
XP_016865452.1:p.Asp5429Glu
|
|
XM_017009964.2:c.16284T>G
|
XP_016865453.1:p.Asp5428Glu
|
|
XM_017009965.1:c.16284T>G
|
XP_016865454.1:p.Asp5428Glu
|
|
XM_017009966.2:c.16206T>G
|
XP_016865455.1:p.Asp5402Glu
|
|
XM_017009967.1:c.16191T>G
|
XP_016865456.1:p.Asp5397Glu
|
|
XM_017009968.2:c.16107T>G
|
XP_016865457.1:p.Asp5369Glu
|
|
XM_017009969.2:c.16287T>G
|
XP_016865458.1:p.Asp5429Glu
|
|
XM_017009972.1:c.9405T>G
|
XP_016865461.1:p.Asp3135Glu
|
|
XM_017009973.1:c.9384T>G
|
XP_016865462.1:p.Asp3128Glu
|
|
NR_003149.2:n.16282T>G
|
|
|