ENST00000461280.2:n.613G>T
|
|
|
ENST00000684116.1:n.208G>T
|
|
|
ENST00000684241.1:n.2148G>T
|
|
|
ENST00000262186.10:c.1315G>T
MANE Select
|
ENSP00000262186.5:p.Gly439Cys
|
|
ENST00000330883.9:c.295G>T
|
ENSP00000328531.4:p.Gly99Cys
|
|
ENST00000262186.9:c.1315G>T
|
ENSP00000262186.5:p.Gly439Cys
|
|
ENST00000330883.8:c.295G>T
|
ENSP00000328531.4:p.Gly99Cys
|
|
ENST00000430723.4:c.967G>T
|
ENSP00000387657.4:p.Gly323Cys
|
|
ENST00000461280.1:n.602G>T
|
|
|
ENST00000473610.5:n.620G>T
|
|
|
ENST00000532957.5:n.1538G>T
|
|
|
NM_000238.3:c.1315G>T , LRG_288t1:c.1315G>T
|
NP_000229.1:p.Gly439Cys
|
|
NM_001204798.1:c.295G>T
|
NP_001191727.1:p.Gly99Cys
|
|
NM_172056.2:c.1315G>T , LRG_288t2:c.1315G>T
|
NP_742053.1:p.Gly439Cys
|
|
NM_172057.2:c.295G>T , LRG_288t3:c.295G>T
|
NP_742054.1:p.Gly99Cys
|
|
XM_011516185.1:c.1015G>T
|
XP_011514487.1:p.Gly339Cys
|
|
XM_011516186.1:c.1315G>T
|
XP_011514488.1:p.Gly439Cys
|
|
XM_011516185.2:c.1015G>T
|
XP_011514487.1:p.Gly339Cys
|
|
XM_011516186.3:c.1315G>T
|
XP_011514488.1:p.Gly439Cys
|
|
XM_017012195.1:c.1165G>T
|
XP_016867684.1:p.Gly389Cys
|
|
XM_017012196.1:c.1138G>T
|
XP_016867685.1:p.Gly380Cys
|
|
NM_000238.4:c.1315G>T
MANE Select
|
NP_000229.1:p.Gly439Cys
|
|
NM_001204798.2:c.295G>T
|
NP_001191727.1:p.Gly99Cys
|
|
NM_172057.3:c.295G>T
|
NP_742054.1:p.Gly99Cys
|
|