ENST00000370192.8:c.2029G>C
MANE Select
|
ENSP00000359211.3:p.Glu677Gln
|
|
ENST00000370192.7:c.2029G>C
|
ENSP00000359211.3:p.Glu677Gln
|
|
NM_000110.3:c.2029G>C , LRG_722t1:c.2029G>C
|
NP_000101.2:p.Glu677Gln
|
|
XM_005270562.3:c.1813G>C
|
XP_005270619.2:p.Glu605Gln
|
|
XM_006710397.2:c.2029G>C
|
XP_006710460.1:p.Glu677Gln
|
|
XR_947619.1:n.1125-1938C>G
|
|
|
XR_947620.1:n.1124+6389C>G
|
|
|
XR_947621.1:n.1125-1938C>G
|
|
|
XM_006710397.3:c.2029G>C
|
XP_006710460.1:p.Glu677Gln
|
|
XM_017000507.1:c.1918G>C
|
XP_016855996.1:p.Glu640Gln
|
|
XM_017000508.2:c.1534G>C
|
XP_016855997.1:p.Glu512Gln
|
|
XM_017000509.2:c.1534G>C
|
XP_016855998.1:p.Glu512Gln
|
|
XM_017000510.1:c.1534G>C
|
XP_016855999.1:p.Glu512Gln
|
|
NM_000110.4:c.2029G>C
MANE Select
|
NP_000101.2:p.Glu677Gln
|
|