ENST00000370192.8:c.1907T>G
MANE Select
|
ENSP00000359211.3:p.Ile636Ser
|
|
ENST00000370192.7:c.1907T>G
|
ENSP00000359211.3:p.Ile636Ser
|
|
NM_000110.3:c.1907T>G , LRG_722t1:c.1907T>G
|
NP_000101.2:p.Ile636Ser
|
|
XM_005270562.3:c.1691T>G
|
XP_005270619.2:p.Ile564Ser
|
|
XM_006710397.2:c.1907T>G
|
XP_006710460.1:p.Ile636Ser
|
|
XR_947619.1:n.1347-1174A>C
|
|
|
XR_947620.1:n.1125-1174A>C
|
|
|
XR_947621.1:n.1347-1174A>C
|
|
|
XM_006710397.3:c.1907T>G
|
XP_006710460.1:p.Ile636Ser
|
|
XM_017000507.1:c.1796T>G
|
XP_016855996.1:p.Ile599Ser
|
|
XM_017000508.2:c.1412T>G
|
XP_016855997.1:p.Ile471Ser
|
|
XM_017000509.2:c.1412T>G
|
XP_016855998.1:p.Ile471Ser
|
|
XM_017000510.1:c.1412T>G
|
XP_016855999.1:p.Ile471Ser
|
|
XR_001737686.2:n.692-1174A>C
|
|
|
XR_001737687.1:n.692-1174A>C
|
|
|
XR_001737688.2:n.692-1174A>C
|
|
|
NM_000110.4:c.1907T>G
MANE Select
|
NP_000101.2:p.Ile636Ser
|
|