ENST00000476379.6:c.517-117T>G
MANE Select
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ENSP00000417960.2:n.517-117T>G
|
|
ENST00000650641.1:n.596-117T>G
|
|
|
ENST00000650889.1:n.689-117T>G
|
|
|
ENST00000651046.1:c.517-117T>G
|
ENSP00000499175.1:n.517-117T>G
|
|
ENST00000651818.1:n.659-117T>G
|
|
|
ENST00000652024.1:n.608-117T>G
|
|
|
ENST00000652408.1:n.654-117T>G
|
|
|
ENST00000442201.6:c.517-117T>G
|
ENSP00000405708.2:n.517-117T>G
|
|
ENST00000476379.5:c.517-117T>G
|
ENSP00000417960.1:n.517-117T>G
|
|
NM_181426.1:c.517-117T>G
|
NP_852091.1:n.517-117T>G
|
|
NM_181426.2:c.517-117T>G
MANE Select
|
NP_852091.1:n.517-117T>G
|
|