|
ENST00000486121.7:c.*226G>C
(GLA)
|
ENSP00000501124.2:n.*226G>C
|
|
|
ENST00000674127.2:c.*283G>C
(GLA)
|
ENSP00000501044.2:n.*283G>C
|
|
|
ENST00000710365.1:c.855G>C
(GLA)
|
ENSP00000518234.1:p.Gly285=
|
|
|
ENST00000218516.4:c.780G>C
(GLA)
MANE Select
|
ENSP00000218516.4:p.Gly260=
|
|
|
ENST00000466414.2:n.699G>C
(GLA)
|
|
|
|
ENST00000468823.2:n.1715G>C
(GLA)
|
|
|
|
ENST00000479445.2:n.1177G>C
(GLA)
|
|
|
|
ENST00000480513.6:c.*88G>C
(GLA)
|
ENSP00000497055.1:n.*88G>C
|
|
|
ENST00000486121.6:c.825G>C
(GLA)
|
|
|
|
ENST00000649178.1:c.903G>C
(GLA)
|
ENSP00000498186.1:p.Gly301=
|
|
|
ENST00000674127.1:c.880G>C
(GLA)
|
ENSP00000501044.1:n.880G>C
|
|
|
ENST00000674142.1:n.867G>C
(GLA)
|
|
|
|
ENST00000674634.2:c.780G>C
(GLA)
|
ENSP00000502629.2:p.Gly260=
|
|
|
ENST00000675592.1:c.780G>C
(GLA)
|
ENSP00000502239.1:p.Gly260=
|
|
|
ENST00000675799.1:c.*88G>C
(GLA)
|
ENSP00000502661.1:n.*88G>C
|
|
|
ENST00000675968.1:n.3434G>C
(GLA)
|
|
|
|
ENST00000676156.1:c.744G>C
(GLA)
|
ENSP00000501730.1:p.Gly248=
|
|
|
ENST00000676372.1:c.780G>C
(GLA)
|
ENSP00000502805.1:p.Gly260=
|
|
|
ENST00000218516.3:c.780G>C
(GLA)
|
ENSP00000218516.3:p.Gly260=
|
|
|
ENST00000409170.3:c.300+3349C>G
(RPL36A-HNRNPH2)
|
ENSP00000386655.4:n.300+3349C>G
|
|
|
ENST00000409338.5:c.177+6984C>G
(RPL36A-HNRNPH2)
|
ENSP00000386974.2:n.177+6984C>G
|
|
|
ENST00000468823.1:n.329G>C
(GLA)
|
|
|
|
ENST00000493905.6:c.*168G>C
(GLA)
|
ENSP00000476935.1:n.*168G>C
|
|
|
NM_000169.2:c.780G>C , LRG_672t1:c.780G>C
(GLA)
|
NP_000160.1:p.Gly260=
|
|
|
NM_001199973.1:c.408+3349C>G
(RPL36A-HNRNPH2)
|
NP_001186902.1:n.408+3349C>G
|
|
|
NM_001199974.1:c.285+6984C>G
(RPL36A-HNRNPH2)
|
NP_001186903.1:n.285+6984C>G
|
|
|
XR_938397.1:n.865G>C
(GLA)
|
|
|
|
XR_938397.2:n.886G>C
(GLA)
|
|
|
|
NM_001199973.2:c.300+3349C>G
(RPL36A-HNRNPH2)
|
NP_001186902.2:n.300+3349C>G
|
|
|
NM_001199974.2:c.177+6984C>G
(RPL36A-HNRNPH2)
|
NP_001186903.2:n.177+6984C>G
|
|
|
NM_000169.3:c.780G>C
(GLA)
MANE Select
|
NP_000160.1:p.Gly260=
|
|
|
NR_164783.1:n.859G>C
(GLA)
|
|
|
