ENST00000394867.9:n.1485+111G>A
|
|
|
ENST00000688002.1:n.3197+111G>A
|
|
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ENST00000688751.1:n.182+111G>A
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|
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ENST00000689792.1:n.950+111G>A
|
|
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ENST00000262948.10:c.1046+111G>A
MANE Select
|
ENSP00000262948.4:n.1046+111G>A
|
|
ENST00000262948.9:c.1046+111G>A
|
ENSP00000262948.3:n.1046+111G>A
|
|
ENST00000394867.8:c.755+111G>A
|
ENSP00000378336.1:n.755+111G>A
|
|
ENST00000597263.5:n.231+111G>A
|
|
|
ENST00000599021.1:c.156+111G>A
|
|
|
ENST00000600584.5:n.1717G>A
|
|
|
ENST00000601786.5:n.1347+111G>A
|
|
|
NM_030662.3:c.1046+111G>A , LRG_750t1:c.1046+111G>A
|
NP_109587.1:n.1046+111G>A
|
|
XM_006722799.2:c.767+111G>A
|
XP_006722862.1:n.767+111G>A
|
|
XM_011528133.1:c.476+111G>A
|
XP_011526435.1:n.476+111G>A
|
|
XM_017026989.1:c.1046+111G>A
|
XP_016882478.1:n.1046+111G>A
|
|
XM_017026990.1:c.767+111G>A
|
XP_016882479.1:n.767+111G>A
|
|
NM_030662.4:c.1046+111G>A
MANE Select
|
NP_109587.1:n.1046+111G>A
|
|