ENST00000486121.7:c.*86-133G>A
(GLA)
|
ENSP00000501124.2:n.*86-133G>A
|
|
ENST00000674127.2:c.*143-133G>A
(GLA)
|
ENSP00000501044.2:n.*143-133G>A
|
|
ENST00000710365.1:c.715-133G>A
(GLA)
|
ENSP00000518234.1:n.715-133G>A
|
|
ENST00000218516.4:c.640-133G>A
(GLA)
MANE Select
|
ENSP00000218516.4:n.640-133G>A
|
|
ENST00000466414.2:n.559-133G>A
(GLA)
|
|
|
ENST00000468823.2:n.1575-133G>A
(GLA)
|
|
|
ENST00000479445.2:n.1037-133G>A
(GLA)
|
|
|
ENST00000480513.6:c.548-133G>A
(GLA)
|
ENSP00000497055.1:n.548-133G>A
|
|
ENST00000486121.6:c.685-133G>A
(GLA)
|
|
|
ENST00000649178.1:c.763-133G>A
(GLA)
|
ENSP00000498186.1:n.763-133G>A
|
|
ENST00000674127.1:c.740-133G>A
(GLA)
|
ENSP00000501044.1:n.740-133G>A
|
|
ENST00000674142.1:n.727-133G>A
(GLA)
|
|
|
ENST00000674634.2:c.640-133G>A
(GLA)
|
ENSP00000502629.2:n.640-133G>A
|
|
ENST00000675592.1:c.640-133G>A
(GLA)
|
ENSP00000502239.1:n.640-133G>A
|
|
ENST00000675799.1:c.548-133G>A
(GLA)
|
ENSP00000502661.1:n.548-133G>A
|
|
ENST00000675968.1:n.3161G>A
(GLA)
|
|
|
ENST00000676156.1:c.604-133G>A
(GLA)
|
ENSP00000501730.1:n.604-133G>A
|
|
ENST00000676372.1:c.640-133G>A
(GLA)
|
ENSP00000502805.1:n.640-133G>A
|
|
ENST00000218516.3:c.640-133G>A
(GLA)
|
ENSP00000218516.3:n.640-133G>A
|
|
ENST00000409170.3:c.300+3622C>T
(RPL36A-HNRNPH2)
|
ENSP00000386655.4:n.300+3622C>T
|
|
ENST00000409338.5:c.177+7257C>T
(RPL36A-HNRNPH2)
|
ENSP00000386974.2:n.177+7257C>T
|
|
ENST00000468823.1:n.189-133G>A
(GLA)
|
|
|
ENST00000480513.5:n.478-133G>A
(GLA)
|
|
|
ENST00000486121.5:n.685-133G>A
(GLA)
|
|
|
ENST00000493905.6:c.*28-133G>A
(GLA)
|
ENSP00000476935.1:n.*28-133G>A
|
|
NM_000169.2:c.640-133G>A , LRG_672t1:c.640-133G>A
(GLA)
|
NP_000160.1:n.640-133G>A
|
|
NM_001199973.1:c.408+3622C>T
(RPL36A-HNRNPH2)
|
NP_001186902.1:n.408+3622C>T
|
|
NM_001199974.1:c.285+7257C>T
(RPL36A-HNRNPH2)
|
NP_001186903.1:n.285+7257C>T
|
|
XR_938397.1:n.725-133G>A
(GLA)
|
|
|
XR_938397.2:n.746-133G>A
(GLA)
|
|
|
NM_001199973.2:c.300+3622C>T
(RPL36A-HNRNPH2)
|
NP_001186902.2:n.300+3622C>T
|
|
NM_001199974.2:c.177+7257C>T
(RPL36A-HNRNPH2)
|
NP_001186903.2:n.177+7257C>T
|
|
NM_000169.3:c.640-133G>A
(GLA)
MANE Select
|
NP_000160.1:n.640-133G>A
|
|
NR_164783.1:n.719-133G>A
(GLA)
|
|
|