|
ENST00000703936.1:c.2668C>T
|
ENSP00000515567.1:p.Pro890Ser
|
|
|
ENST00000703937.1:c.*1729C>T
|
ENSP00000515568.1:n.*1729C>T
|
|
|
ENST00000326739.9:c.628C>T
MANE Select
|
ENSP00000321584.4:p.Pro210Ser
|
|
|
ENST00000429182.6:c.628C>T
|
ENSP00000393525.2:p.Pro210Ser
|
|
|
ENST00000442157.2:c.553C>T
|
ENSP00000403502.2:p.Pro185Ser
|
|
|
ENST00000462980.2:n.1143C>T
|
|
|
|
ENST00000472328.2:n.694C>T
|
|
|
|
ENST00000491610.2:n.588C>T
|
|
|
|
ENST00000676607.1:n.924C>T
|
|
|
|
ENST00000676627.1:n.1358C>T
|
|
|
|
ENST00000676708.1:n.1908C>T
|
|
|
|
ENST00000676864.1:n.1777C>T
|
|
|
|
ENST00000677010.1:c.664C>T
|
ENSP00000503089.1:p.Pro222Ser
|
|
|
ENST00000677108.1:n.2534C>T
|
|
|
|
ENST00000677168.1:n.1100C>T
|
|
|
|
ENST00000677185.1:n.1191C>T
|
|
|
|
ENST00000677205.1:n.1412C>T
|
|
|
|
ENST00000677344.1:n.1902C>T
|
|
|
|
ENST00000677480.1:c.*305C>T
|
ENSP00000504378.1:n.*305C>T
|
|
|
ENST00000677519.1:n.1338C>T
|
|
|
|
ENST00000677593.1:n.1184C>T
|
|
|
|
ENST00000677740.1:n.2133C>T
|
|
|
|
ENST00000677991.1:n.1801C>T
|
|
|
|
ENST00000678001.1:n.1121C>T
|
|
|
|
ENST00000678085.1:n.1184C>T
|
|
|
|
ENST00000678177.1:n.2477C>T
|
|
|
|
ENST00000678603.1:n.1706C>T
|
|
|
|
ENST00000678724.1:c.553C>T
|
ENSP00000503874.1:p.Pro185Ser
|
|
|
ENST00000678920.1:n.786C>T
|
|
|
|
ENST00000679019.1:n.1398C>T
|
|
|
|
ENST00000679117.1:c.*443C>T
|
ENSP00000503240.1:n.*443C>T
|
|
|
ENST00000679339.1:n.1469C>T
|
|
|
|
ENST00000326739.8:c.628C>T
|
ENSP00000321584.4:p.Pro210Ser
|
|
|
ENST00000429182.5:c.422C>T
|
|
|
|
ENST00000442157.1:c.553C>T
|
ENSP00000403502.1:p.Pro185Ser
|
|
|
ENST00000462980.1:n.530C>T
|
|
|
|
ENST00000491610.1:n.588C>T
|
|
|
|
NM_000884.2:c.628C>T
|
NP_000875.2:p.Pro210Ser
|
|
|
XM_006713128.2:c.838C>T
|
XP_006713191.1:p.Pro280Ser
|
|
|
XM_006713128.3:c.838C>T
|
XP_006713191.1:p.Pro280Ser
|
|
|
XM_017006349.1:c.763C>T
|
XP_016861838.1:p.Pro255Ser
|
|
|
XM_017006350.1:c.763C>T
|
XP_016861839.1:p.Pro255Ser
|
|
|
NM_000884.3:c.628C>T
MANE Select
|
NP_000875.2:p.Pro210Ser
|
|
