|
ENST00000703936.1:c.2707G>T
|
ENSP00000515567.1:p.Ala903Ser
|
|
|
ENST00000703937.1:c.*1768G>T
|
ENSP00000515568.1:n.*1768G>T
|
|
|
ENST00000326739.9:c.667G>T
MANE Select
|
ENSP00000321584.4:p.Ala223Ser
|
|
|
ENST00000429182.6:c.667G>T
|
ENSP00000393525.2:p.Ala223Ser
|
|
|
ENST00000442157.2:c.592G>T
|
ENSP00000403502.2:p.Ala198Ser
|
|
|
ENST00000462980.2:n.1182G>T
|
|
|
|
ENST00000472328.2:n.733G>T
|
|
|
|
ENST00000491610.2:n.627G>T
|
|
|
|
ENST00000676607.1:n.963G>T
|
|
|
|
ENST00000676627.1:n.1397G>T
|
|
|
|
ENST00000676708.1:n.1947G>T
|
|
|
|
ENST00000676864.1:n.1816G>T
|
|
|
|
ENST00000677010.1:c.703G>T
|
ENSP00000503089.1:p.Ala235Ser
|
|
|
ENST00000677108.1:n.2573G>T
|
|
|
|
ENST00000677168.1:n.1139G>T
|
|
|
|
ENST00000677185.1:n.1230G>T
|
|
|
|
ENST00000677205.1:n.1451G>T
|
|
|
|
ENST00000677344.1:n.1941G>T
|
|
|
|
ENST00000677480.1:c.*344G>T
|
ENSP00000504378.1:n.*344G>T
|
|
|
ENST00000677519.1:n.1377G>T
|
|
|
|
ENST00000677593.1:n.1223G>T
|
|
|
|
ENST00000677740.1:n.2172G>T
|
|
|
|
ENST00000677991.1:n.1840G>T
|
|
|
|
ENST00000678001.1:n.1160G>T
|
|
|
|
ENST00000678085.1:n.1223G>T
|
|
|
|
ENST00000678177.1:n.2516G>T
|
|
|
|
ENST00000678603.1:n.1745G>T
|
|
|
|
ENST00000678724.1:c.592G>T
|
ENSP00000503874.1:p.Ala198Ser
|
|
|
ENST00000678920.1:n.825G>T
|
|
|
|
ENST00000679019.1:n.1437G>T
|
|
|
|
ENST00000679117.1:c.*482G>T
|
ENSP00000503240.1:n.*482G>T
|
|
|
ENST00000679339.1:n.1508G>T
|
|
|
|
ENST00000326739.8:c.667G>T
|
ENSP00000321584.4:p.Ala223Ser
|
|
|
ENST00000429182.5:c.461G>T
|
|
|
|
ENST00000442157.1:c.592G>T
|
ENSP00000403502.1:p.Ala198Ser
|
|
|
ENST00000462980.1:n.569G>T
|
|
|
|
ENST00000491610.1:n.627G>T
|
|
|
|
NM_000884.2:c.667G>T
|
NP_000875.2:p.Ala223Ser
|
|
|
XM_006713128.2:c.877G>T
|
XP_006713191.1:p.Ala293Ser
|
|
|
XM_006713128.3:c.877G>T
|
XP_006713191.1:p.Ala293Ser
|
|
|
XM_017006349.1:c.802G>T
|
XP_016861838.1:p.Ala268Ser
|
|
|
XM_017006350.1:c.802G>T
|
XP_016861839.1:p.Ala268Ser
|
|
|
NM_000884.3:c.667G>T
MANE Select
|
NP_000875.2:p.Ala223Ser
|
|
