ENST00000298912.9:c.886-1071C>A
MANE Select
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ENSP00000298912.3:n.886-1071C>A
|
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ENST00000298912.8:c.886-1071C>A
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ENSP00000298912.3:n.886-1071C>A
|
|
ENST00000556454.1:n.250-1071C>A
|
|
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NM_024734.3:c.886-1071C>A
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NP_079010.2:n.886-1071C>A
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XM_011537158.1:c.886-1071C>A
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XP_011535460.1:n.886-1071C>A
|
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XM_011537159.1:c.886-1071C>A
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XP_011535461.1:n.886-1071C>A
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XR_245721.2:n.998-1071C>A
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|
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XR_429330.2:n.998-1071C>A
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|
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XR_429332.2:n.998-1071C>A
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|
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XM_011537159.2:c.886-1071C>A
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XP_011535461.1:n.886-1071C>A
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|
XM_017021646.1:c.826-1071C>A
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XP_016877135.1:n.826-1071C>A
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|
XM_017021647.1:c.886-1071C>A
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XP_016877136.1:n.886-1071C>A
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XR_001750558.1:n.998-1071C>A
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|
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NM_024734.4:c.886-1071C>A
MANE Select
|
NP_079010.2:n.886-1071C>A
|
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