ENST00000272321.12:c.1066T>A
MANE Select
|
ENSP00000272321.7:p.Cys356Ser
|
|
ENST00000272321.11:c.1066T>A
|
ENSP00000272321.7:p.Cys356Ser
|
|
ENST00000398544.7:c.589T>A
|
ENSP00000381552.3:p.Cys197Ser
|
|
ENST00000409120.5:c.490T>A
|
ENSP00000386769.1:p.Cys164Ser
|
|
ENST00000409199.5:c.490T>A
|
ENSP00000386592.1:p.Cys164Ser
|
|
ENST00000409354.6:c.427T>A
|
ENSP00000386795.2:p.Cys143Ser
|
|
ENST00000409562.7:c.1066T>A
|
ENSP00000387222.3:p.Cys356Ser
|
|
ENST00000409835.5:n.1313T>A
|
|
|
ENST00000417238.5:c.*1177T>A
|
ENSP00000411429.1:n.*1177T>A
|
|
ENST00000493315.1:n.768T>A
|
|
|
NM_001042692.2:c.589T>A
|
NP_001036157.1:p.Cys197Ser
|
|
NM_015910.5:c.1066T>A
|
NP_056994.3:p.Cys356Ser
|
|
NR_122106.1:n.713T>A
|
|
|
XM_005264348.2:c.1066T>A
|
XP_005264405.1:p.Cys356Ser
|
|
XM_011532881.1:c.994T>A
|
XP_011531183.1:p.Cys332Ser
|
|
XM_011532882.1:c.967T>A
|
XP_011531184.1:p.Cys323Ser
|
|
XM_011532883.1:c.1066T>A
|
XP_011531185.1:p.Cys356Ser
|
|
XM_011532884.1:c.1066T>A
|
XP_011531186.1:p.Cys356Ser
|
|
XM_011532885.1:c.1066T>A
|
XP_011531187.1:p.Cys356Ser
|
|
XM_011532886.1:c.1066T>A
|
XP_011531188.1:p.Cys356Ser
|
|
XM_011532887.1:c.1066T>A
|
XP_011531189.1:p.Cys356Ser
|
|
XM_011532888.1:c.1066T>A
|
XP_011531190.1:p.Cys356Ser
|
|
XM_011532889.1:c.1066T>A
|
XP_011531191.1:p.Cys356Ser
|
|
XM_011532890.1:c.1066T>A
|
XP_011531192.1:p.Cys356Ser
|
|
XM_011532891.1:c.994T>A
|
XP_011531193.1:p.Cys332Ser
|
|
XR_244934.1:n.1313T>A
|
|
|
XR_244935.1:n.1313T>A
|
|
|
XR_939686.1:n.1313T>A
|
|
|
NM_001042692.3:c.589T>A
|
NP_001036157.1:p.Cys197Ser
|
|
NM_001354044.1:c.994T>A
|
NP_001340973.1:p.Cys332Ser
|
|
NM_001354045.1:c.1066T>A
|
NP_001340974.1:p.Cys356Ser
|
|
NM_015910.6:c.1066T>A
|
NP_056994.3:p.Cys356Ser
|
|
NR_122106.2:n.713T>A
|
|
|
NR_148704.1:n.1846T>A
|
|
|
NR_148705.1:n.1594T>A
|
|
|
XM_005264348.4:c.1066T>A
|
XP_005264405.1:p.Cys356Ser
|
|
XM_011532881.3:c.994T>A
|
XP_011531183.1:p.Cys332Ser
|
|
XM_011532884.3:c.1066T>A
|
XP_011531186.1:p.Cys356Ser
|
|
XM_011532887.3:c.1066T>A
|
XP_011531189.1:p.Cys356Ser
|
|
XM_011532890.3:c.1066T>A
|
XP_011531192.1:p.Cys356Ser
|
|
XM_011532891.2:c.994T>A
|
XP_011531193.1:p.Cys332Ser
|
|
XM_017004253.2:c.1066T>A
|
XP_016859742.1:p.Cys356Ser
|
|
XM_017004254.2:c.1066T>A
|
XP_016859743.1:p.Cys356Ser
|
|
XR_001738759.2:n.1528T>A
|
|
|
XR_001738760.2:n.1528T>A
|
|
|
XR_002959303.1:n.1528T>A
|
|
|
XR_244934.3:n.1528T>A
|
|
|
NM_015910.7:c.1066T>A
MANE Select
|
NP_056994.3:p.Cys356Ser
|
|
NM_001354044.2:c.994T>A
|
NP_001340973.1:p.Cys332Ser
|
|
NM_001354045.2:c.1066T>A
|
NP_001340974.1:p.Cys356Ser
|
|
NR_148704.2:n.1524T>A
|
|
|
NR_148705.2:n.1272T>A
|
|
|