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ENST00000651735.1:c.-8-9598A=
MANE Select
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ENSP00000498313.1:n.-8-9598A=
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ENST00000652098.1:c.-17-35776A=
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
NP_056953.2:n.83-9598A=
|
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|
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|
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|
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XM_011533840.1:c.-2-9598A=
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|
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|
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|
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|
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|
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|
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|
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|
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|
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XM_011533842.2:c.83-9598A=
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XP_011532144.1:n.83-9598A=
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XM_011533843.2:c.83-9598A=
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XP_011532145.1:n.83-9598A=
|
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|
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|
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|
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|
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|
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|
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|
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NM_001354666.2:c.-2-9598A=
|
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|
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|
NP_001341596.1:n.-2-9598A=
|
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NM_001354668.2:c.83-9598A=
|
NP_001341597.1:n.83-9598A=
|
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NM_001354669.2:c.-435-9598A=
|
NP_001341598.1:n.-435-9598A=
|
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NM_001354670.2:c.-2-9598A=
|
NP_001341599.1:n.-2-9598A=
|
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NM_001374261.1:c.-2-9598A=
|
NP_001361190.1:n.-2-9598A=
|
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|
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|
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|
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|
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NM_001374264.1:c.-2-9598A=
|
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|
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|
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|
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|
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|
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|
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|
|
NM_015869.5:c.83-9598A=
|
NP_056953.2:n.83-9598A=
|
|
NM_138711.4:c.-2-9598A=
|
NP_619725.2:n.-2-9598A=
|
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NM_138712.4:c.-2-9598A=
|
NP_619726.2:n.-2-9598A=
|
|
NM_001330615.4:c.-8-9598A=
|
NP_001317544.2:n.-8-9598A=
|
|
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|
NP_001341595.2:n.-8-9598A=
|
|
NM_001354667.3:c.-8-9598A=
|
NP_001341596.2:n.-8-9598A=
|
|
NM_001374261.3:c.-8-9598A=
|
NP_001361190.2:n.-8-9598A=
|
|
NM_001374262.3:c.-8-9598A=
|
NP_001361191.2:n.-8-9598A=
|
|
NM_001374263.2:c.-8-9598A=
|
NP_001361192.2:n.-8-9598A=
|
|
NM_001374264.2:c.-8-9598A=
|
NP_001361193.2:n.-8-9598A=
|
|
NM_005037.7:c.-8-9598A=
|
NP_005028.5:n.-8-9598A=
|
|
NM_138711.6:c.-8-9598A=
MANE Select
|
NP_619725.3:n.-8-9598A=
|
|
NM_138712.5:c.-8-9598A=
|
NP_619726.3:n.-8-9598A=
|
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