ENST00000370192.8:c.1970C>G
MANE Select
|
ENSP00000359211.3:p.Ser657Cys
|
|
ENST00000370192.7:c.1970C>G
|
ENSP00000359211.3:p.Ser657Cys
|
|
NM_000110.3:c.1970C>G , LRG_722t1:c.1970C>G
|
NP_000101.2:p.Ser657Cys
|
|
XM_005270562.3:c.1754C>G
|
XP_005270619.2:p.Ser585Cys
|
|
XM_006710397.2:c.1970C>G
|
XP_006710460.1:p.Ser657Cys
|
|
XR_947619.1:n.1347-1237G>C
|
|
|
XR_947620.1:n.1125-1237G>C
|
|
|
XR_947621.1:n.1347-1237G>C
|
|
|
XM_006710397.3:c.1970C>G
|
XP_006710460.1:p.Ser657Cys
|
|
XM_017000507.1:c.1859C>G
|
XP_016855996.1:p.Ser620Cys
|
|
XM_017000508.2:c.1475C>G
|
XP_016855997.1:p.Ser492Cys
|
|
XM_017000509.2:c.1475C>G
|
XP_016855998.1:p.Ser492Cys
|
|
XM_017000510.1:c.1475C>G
|
XP_016855999.1:p.Ser492Cys
|
|
XR_001737686.2:n.692-1237G>C
|
|
|
XR_001737687.1:n.692-1237G>C
|
|
|
XR_001737688.2:n.692-1237G>C
|
|
|
NM_000110.4:c.1970C>G
MANE Select
|
NP_000101.2:p.Ser657Cys
|
|