ENST00000486121.7:c.662+182C>A
(GLA)
|
ENSP00000501124.2:n.662+182C>A
|
|
ENST00000674127.2:c.662+182C>A
(GLA)
|
ENSP00000501044.2:n.662+182C>A
|
|
ENST00000710365.1:c.623-294C>A
(GLA)
|
ENSP00000518234.1:n.623-294C>A
|
|
ENST00000218516.4:c.548-294C>A
(GLA)
MANE Select
|
ENSP00000218516.4:n.548-294C>A
|
|
ENST00000466414.2:n.467-294C>A
(GLA)
|
|
|
ENST00000468823.2:n.1189C>A
(GLA)
|
|
|
ENST00000479445.2:n.944+182C>A
(GLA)
|
|
|
ENST00000480513.6:c.547+581C>A
(GLA)
|
ENSP00000497055.1:n.547+581C>A
|
|
ENST00000486121.6:c.592+182C>A
(GLA)
|
|
|
ENST00000649178.1:c.671-294C>A
(GLA)
|
ENSP00000498186.1:n.671-294C>A
|
|
ENST00000674127.1:c.590+182C>A
(GLA)
|
ENSP00000501044.1:n.590+182C>A
|
|
ENST00000674142.1:n.635-294C>A
(GLA)
|
|
|
ENST00000674634.2:c.548-294C>A
(GLA)
|
ENSP00000502629.2:n.548-294C>A
|
|
ENST00000675592.1:c.548-294C>A
(GLA)
|
ENSP00000502239.1:n.548-294C>A
|
|
ENST00000675799.1:c.547+581C>A
(GLA)
|
ENSP00000502661.1:n.547+581C>A
|
|
ENST00000675968.1:n.1189C>A
(GLA)
|
|
|
ENST00000676156.1:c.512-294C>A
(GLA)
|
ENSP00000501730.1:n.512-294C>A
|
|
ENST00000676372.1:c.548-294C>A
(GLA)
|
ENSP00000502805.1:n.548-294C>A
|
|
ENST00000218516.3:c.548-294C>A
(GLA)
|
ENSP00000218516.3:n.548-294C>A
|
|
ENST00000409170.3:c.300+5594G>T
(RPL36A-HNRNPH2)
|
ENSP00000386655.4:n.300+5594G>T
|
|
ENST00000409338.5:c.177+9229G>T
(RPL36A-HNRNPH2)
|
ENSP00000386974.2:n.177+9229G>T
|
|
ENST00000480513.5:n.477+581C>A
(GLA)
|
|
|
ENST00000486121.5:n.592+182C>A
(GLA)
|
|
|
ENST00000493905.6:c.548-294C>A
(GLA)
|
ENSP00000476935.1:n.548-294C>A
|
|
NM_000169.2:c.548-294C>A , LRG_672t1:c.548-294C>A
(GLA)
|
NP_000160.1:n.548-294C>A
|
|
NM_001199973.1:c.408+5594G>T
(RPL36A-HNRNPH2)
|
NP_001186902.1:n.408+5594G>T
|
|
NM_001199974.1:c.285+9229G>T
(RPL36A-HNRNPH2)
|
NP_001186903.1:n.285+9229G>T
|
|
XR_938397.1:n.576-294C>A
(GLA)
|
|
|
XR_938397.2:n.597-294C>A
(GLA)
|
|
|
NM_001199973.2:c.300+5594G>T
(RPL36A-HNRNPH2)
|
NP_001186902.2:n.300+5594G>T
|
|
NM_001199974.2:c.177+9229G>T
(RPL36A-HNRNPH2)
|
NP_001186903.2:n.177+9229G>T
|
|
NM_000169.3:c.548-294C>A
(GLA)
MANE Select
|
NP_000160.1:n.548-294C>A
|
|
NR_164783.1:n.570-294C>A
(GLA)
|
|
|