ENST00000394867.9:n.1531+236G>A
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|
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ENST00000688002.1:n.3243+236G>A
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|
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ENST00000688751.1:n.228+236G>A
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|
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ENST00000689792.1:n.996+236G>A
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|
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ENST00000262948.10:c.1092+236G>A
MANE Select
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ENSP00000262948.4:n.1092+236G>A
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ENST00000262948.9:c.1092+236G>A
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ENSP00000262948.3:n.1092+236G>A
|
|
ENST00000394867.8:c.801+236G>A
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ENSP00000378336.1:n.801+236G>A
|
|
ENST00000597263.5:n.277+236G>A
|
|
|
ENST00000599021.1:c.202+236G>A
|
|
|
ENST00000600584.5:n.2541+236G>A
|
|
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ENST00000601786.5:n.1393+236G>A
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|
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NM_030662.3:c.1092+236G>A , LRG_750t1:c.1092+236G>A
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NP_109587.1:n.1092+236G>A
|
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XM_006722799.2:c.813+236G>A
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XP_006722862.1:n.813+236G>A
|
|
XM_011528133.1:c.522+236G>A
|
XP_011526435.1:n.522+236G>A
|
|
NM_030662.4:c.1092+236G>A
MANE Select
|
NP_109587.1:n.1092+236G>A
|
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