ENST00000405460.9:c.12148G>C
MANE Select
|
ENSP00000384582.2:p.Asp4050His
|
|
ENST00000425867.3:c.1102G>C
|
ENSP00000392618.3:p.Asp368His
|
|
ENST00000639431.1:c.265+87123G>C
|
ENSP00000491057.1:n.265+87123G>C
|
|
ENST00000640464.1:n.2567G>C
|
|
|
ENST00000640729.1:n.725G>C
|
|
|
ENST00000405460.6:c.12148G>C
|
ENSP00000384582.2:p.Asp4050His
|
|
NM_032119.3:c.12148G>C
|
NP_115495.3:p.Asp4050His
|
|
NR_003149.1:n.12161G>C
|
|
|
XM_011543675.1:c.12145G>C
|
XP_011541977.1:p.Asp4049His
|
|
XM_011543676.1:c.12067G>C
|
XP_011541978.1:p.Asp4023His
|
|
XM_011543677.1:c.9451G>C
|
XP_011541979.1:p.Asp3151His
|
|
XM_011543678.1:c.12148G>C
|
XP_011541980.1:p.Asp4050His
|
|
NM_032119.4:c.12148G>C
MANE Select
|
NP_115495.3:p.Asp4050His
|
|
XM_017009963.2:c.12169G>C
|
XP_016865452.1:p.Asp4057His
|
|
XM_017009964.2:c.12166G>C
|
XP_016865453.1:p.Asp4056His
|
|
XM_017009965.1:c.12166G>C
|
XP_016865454.1:p.Asp4056His
|
|
XM_017009966.2:c.12088G>C
|
XP_016865455.1:p.Asp4030His
|
|
XM_017009967.1:c.12073G>C
|
XP_016865456.1:p.Asp4025His
|
|
XM_017009968.2:c.12169G>C
|
XP_016865457.1:p.Asp4057His
|
|
XM_017009969.2:c.12169G>C
|
XP_016865458.1:p.Asp4057His
|
|
XM_017009970.2:c.12169G>C
|
XP_016865459.1:p.Asp4057His
|
|
XM_017009971.2:c.12169G>C
|
XP_016865460.1:p.Asp4057His
|
|
XM_017009972.1:c.5287G>C
|
XP_016865461.1:p.Asp1763His
|
|
XM_017009973.1:c.5266G>C
|
XP_016865462.1:p.Asp1756His
|
|
NR_003149.2:n.12164G>C
|
|
|