ENST00000579774.3:c.*425dup
MANE Select
|
ENSP00000463851.1:n.*425dup
|
|
ENST00000579774.2:c.*425dup
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ENSP00000463851.1:n.*425dup
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ENST00000621517.1:c.*425dup
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ENSP00000484552.1:n.*425dup
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|
NM_005266.6:c.*425dup
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NP_005257.2:n.*425dup
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|
NM_181703.3:c.*425dup
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NP_859054.1:n.*425dup
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XM_005272951.3:c.*425dup
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XP_005273008.1:n.*425dup
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|
XM_011509415.1:c.*425dup
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XP_011507717.1:n.*425dup
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|
XR_922078.1:n.434-19822dup
|
|
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XR_922079.1:n.434-19822dup
|
|
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XM_005272951.4:c.*425dup
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XP_005273008.1:n.*425dup
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|
XM_017001044.1:c.*425dup
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XP_016856533.1:n.*425dup
|
|
XR_922079.3:n.744-19822dup
|
|
|
NM_181703.4:c.*425dup
MANE Select
|
NP_859054.1:n.*425dup
|
|
NM_005266.7:c.*425dup
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NP_005257.2:n.*425dup
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|