ENST00000394867.9:n.1531+215T>G
|
|
|
ENST00000688002.1:n.3243+215T>G
|
|
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ENST00000688751.1:n.228+215T>G
|
|
|
ENST00000689792.1:n.996+215T>G
|
|
|
ENST00000262948.10:c.1092+215T>G
MANE Select
|
ENSP00000262948.4:n.1092+215T>G
|
|
ENST00000262948.9:c.1092+215T>G
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ENSP00000262948.3:n.1092+215T>G
|
|
ENST00000394867.8:c.801+215T>G
|
ENSP00000378336.1:n.801+215T>G
|
|
ENST00000597263.5:n.277+215T>G
|
|
|
ENST00000599021.1:c.202+215T>G
|
|
|
ENST00000600584.5:n.2541+215T>G
|
|
|
ENST00000601786.5:n.1393+215T>G
|
|
|
NM_030662.3:c.1092+215T>G , LRG_750t1:c.1092+215T>G
|
NP_109587.1:n.1092+215T>G
|
|
XM_006722799.2:c.813+215T>G
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XP_006722862.1:n.813+215T>G
|
|
XM_011528133.1:c.522+215T>G
|
XP_011526435.1:n.522+215T>G
|
|
NM_030662.4:c.1092+215T>G
MANE Select
|
NP_109587.1:n.1092+215T>G
|
|