ENST00000356518.7:c.2438G>C
MANE Select
|
ENSP00000348912.3:p.Trp813Ser
|
|
ENST00000350009.6:c.2360G>C
|
ENSP00000322550.5:p.Trp787Ser
|
|
ENST00000356518.6:c.2438G>C
|
ENSP00000348912.2:p.Trp813Ser
|
|
ENST00000379861.8:c.2435G>C
|
ENSP00000369190.4:p.Trp812Ser
|
|
ENST00000466620.5:n.1999G>C
|
|
|
ENST00000483362.1:n.1361G>C
|
|
|
ENST00000617732.1:c.*1122G>C
|
ENSP00000483343.1:n.*1122G>C
|
|
ENST00000619289.4:c.2075G>C
|
ENSP00000484600.1:p.Trp692Ser
|
|
NM_001282447.1:c.2435G>C
|
NP_001269376.1:p.Trp812Ser
|
|
NM_025220.3:c.2438G>C
|
NP_079496.1:p.Trp813Ser
|
|
NM_153202.2:c.2360G>C
|
NP_694882.1:p.Trp787Ser
|
|
XM_005260843.1:c.2477G>C
|
XP_005260900.1:p.Trp826Ser
|
|
XM_006723639.1:c.2474G>C
|
XP_006723702.1:p.Trp825Ser
|
|
XM_006723640.1:c.2468G>C
|
XP_006723703.1:p.Trp823Ser
|
|
XM_011529366.1:c.2474G>C
|
XP_011527668.1:p.Trp825Ser
|
|
XM_011529367.1:c.2435G>C
|
XP_011527669.1:p.Trp812Ser
|
|
XM_011529368.1:c.2399G>C
|
XP_011527670.1:p.Trp800Ser
|
|
XM_011529373.1:c.1475G>C
|
XP_011527675.1:p.Trp492Ser
|
|
XR_937153.1:n.2459G>C
|
|
|
XR_937154.1:n.2459G>C
|
|
|
XR_937155.1:n.2380G>C
|
|
|
XR_937157.1:n.2382G>C
|
|
|
NM_001282447.2:c.2435G>C
|
NP_001269376.1:p.Trp812Ser
|
|
NM_025220.4:c.2438G>C
|
NP_079496.1:p.Trp813Ser
|
|
NM_153202.3:c.2360G>C
|
NP_694882.1:p.Trp787Ser
|
|
XM_011529373.2:c.1475G>C
|
XP_011527675.1:p.Trp492Ser
|
|
XR_001754405.1:n.2546G>C
|
|
|
XR_002958534.1:n.2655G>C
|
|
|
NM_001282447.3:c.2435G>C
|
NP_001269376.1:p.Trp812Ser
|
|
NM_025220.5:c.2438G>C
MANE Select
|
NP_079496.1:p.Trp813Ser
|
|
NM_153202.4:c.2360G>C
|
NP_694882.1:p.Trp787Ser
|
|