ENST00000317447.9:c.1665G>C
|
ENSP00000320646.4:p.Glu555Asp
|
|
ENST00000614302.5:c.1665G>C
MANE Select
|
ENSP00000479130.1:p.Glu555Asp
|
|
ENST00000649953.1:c.1875G>C
|
ENSP00000497456.1:p.Glu625Asp
|
|
ENST00000317447.8:c.1665G>C
|
ENSP00000320646.4:p.Glu555Asp
|
|
ENST00000378345.8:c.870G>C
|
ENSP00000367596.4:p.Glu290Asp
|
|
ENST00000393145.5:n.6575G>C
|
|
|
ENST00000406948.7:c.1665G>C
|
ENSP00000384627.3:p.Glu555Asp
|
|
ENST00000537116.5:n.791G>C
|
|
|
ENST00000537155.1:n.405G>C
|
|
|
ENST00000542688.5:c.*409G>C
|
ENSP00000446281.1:n.*409G>C
|
|
ENST00000614302.4:c.1665G>C
|
ENSP00000479130.1:p.Glu555Asp
|
|
NM_001127214.3:c.1665G>C
|
NP_001120686.1:p.Glu555Asp
|
|
NM_001243279.2:c.1665G>C
|
NP_001230208.1:p.Glu555Asp
|
|
NM_001284316.1:c.870G>C
|
NP_001271245.1:p.Glu290Asp
|
|
NM_174917.4:c.1665G>C
|
NP_777577.2:p.Glu555Asp
|
|
NR_045667.2:n.791G>C
|
|
|
NR_104293.1:n.2099G>C
|
|
|
XR_933239.1:n.2106G>C
|
|
|
XR_933240.1:n.2103G>C
|
|
|
XR_933241.1:n.1860G>C
|
|
|
NR_147928.1:n.2143G>C
|
|
|
NR_147929.1:n.1897G>C
|
|
|
XM_017023020.2:c.-3440G>C
|
XP_016878509.1:n.-3440G>C
|
|
XM_024450187.1:c.870G>C
|
XP_024305955.1:p.Glu290Asp
|
|
XR_001751864.2:n.1912G>C
|
|
|
XR_933240.3:n.2102G>C
|
|
|
NM_001127214.4:c.1665G>C
|
NP_001120686.1:p.Glu555Asp
|
|
NM_001243279.3:c.1665G>C
MANE Select
|
NP_001230208.1:p.Glu555Asp
|
|
NM_001284316.2:c.870G>C
|
NP_001271245.1:p.Glu290Asp
|
|
NM_174917.5:c.1665G>C
|
NP_777577.2:p.Glu555Asp
|
|
NR_104293.2:n.2056G>C
|
|
|
NR_147928.2:n.2100G>C
|
|
|
NR_147929.2:n.1854G>C
|
|
|