ENST00000315491.12:c.*13_*28dup
MANE Select
|
ENSP00000320295.7:n.*13_*28dup
|
|
ENST00000680788.1:n.4787_4802dup
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|
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ENST00000315491.11:c.*13_*28dup
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ENSP00000320295.7:n.*13_*28dup
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ENST00000554444.5:c.*13_*28dup
|
ENSP00000451617.1:n.*13_*28dup
|
|
ENST00000555576.5:c.277+2239_277+2254dup
|
ENSP00000452554.1:n.277+2239_277+2254dup
|
|
ENST00000555609.5:c.*1451_*1466dup
|
ENSP00000451276.1:n.*1451_*1466dup
|
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ENST00000556922.1:c.*13_*28dup
|
ENSP00000451560.1:n.*13_*28dup
|
|
NM_001197181.1:c.*13_*28dup
|
NP_001184110.1:n.*13_*28dup
|
|
NM_006086.3:c.*13_*28dup
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NP_006077.2:n.*13_*28dup
|
|
NM_006086.4:c.*13_*28dup
MANE Select
|
NP_006077.2:n.*13_*28dup
|
|
NM_001197181.2:c.*13_*28dup
|
NP_001184110.1:n.*13_*28dup
|
|