ENST00000282516.13:c.6807T>C
MANE Select
|
ENSP00000282516.8:p.Asp2269=
|
|
ENST00000652901.1:c.6807T>C
|
ENSP00000499536.1:p.Asp2269=
|
|
ENST00000282516.12:c.6807T>C
|
ENSP00000282516.8:p.Asp2269=
|
|
ENST00000448238.2:c.6807T>C
|
ENSP00000406266.2:p.Asp2269=
|
|
ENST00000621733.1:c.1-15424T>C
|
ENSP00000480694.1:n.1-15424T>C
|
|
NM_015384.4:c.6807T>C
|
NP_056199.2:p.Asp2269=
|
|
NM_133433.3:c.6807T>C
|
NP_597677.2:p.Asp2269=
|
|
XM_005248280.2:c.6807T>C
|
XP_005248337.1:p.Asp2269=
|
|
XM_005248282.3:c.6063T>C
|
XP_005248339.2:p.Asp2021=
|
|
XM_006714467.2:c.6807T>C
|
XP_006714530.1:p.Asp2269=
|
|
XM_006714468.1:c.6609T>C
|
XP_006714531.1:p.Asp2203=
|
|
XM_011514014.1:c.6426T>C
|
XP_011512316.1:p.Asp2142=
|
|
XM_011514015.1:c.6807T>C
|
XP_011512317.1:p.Asp2269=
|
|
XM_005248280.3:c.6807T>C
|
XP_005248337.1:p.Asp2269=
|
|
XM_005248282.5:c.6147T>C
|
XP_005248339.3:p.Asp2049=
|
|
XM_006714468.2:c.6609T>C
|
XP_006714531.1:p.Asp2203=
|
|
XM_017009329.1:c.6807T>C
|
XP_016864818.1:p.Asp2269=
|
|
XM_017009330.2:c.5190T>C
|
XP_016864819.1:p.Asp1730=
|
|
XM_017009331.1:c.5181T>C
|
XP_016864820.1:p.Asp1727=
|
|
NM_133433.4:c.6807T>C
MANE Select
|
NP_597677.2:p.Asp2269=
|
|
NM_015384.5:c.6807T>C
|
NP_056199.2:p.Asp2269=
|
|