|
ENST00000415928.6:c.665+1052T>C
|
ENSP00000388838.2:n.665+1052T>C
|
|
|
ENST00000435065.7:c.763T>C
|
ENSP00000402760.2:p.Ser255Pro
|
|
|
ENST00000448810.6:c.691T>C
|
ENSP00000401860.2:p.Ser231Pro
|
|
|
ENST00000686757.1:c.710T>C
|
ENSP00000510721.1:p.Leu237Pro
|
|
|
ENST00000687740.1:n.1851T>C
|
|
|
|
ENST00000688151.1:n.1883T>C
|
|
|
|
ENST00000689271.1:c.671+1046T>C
|
ENSP00000510797.1:n.671+1046T>C
|
|
|
ENST00000690900.1:c.672-10T>C
|
ENSP00000510703.1:n.672-10T>C
|
|
|
ENST00000692212.1:n.517T>C
|
|
|
|
ENST00000692355.1:c.204+1065T>C
|
|
|
|
ENST00000692413.1:c.710T>C
|
ENSP00000509374.1:p.Leu237Pro
|
|
|
ENST00000692825.1:c.759T>C
|
ENSP00000509447.1:n.759T>C
|
|
|
ENST00000693308.1:c.704T>C
|
ENSP00000509770.1:p.Leu235Pro
|
|
|
ENST00000693763.1:n.1851T>C
|
|
|
|
ENST00000245407.8:c.691T>C
MANE Select
|
ENSP00000245407.3:p.Ser231Pro
|
|
|
ENST00000245407.7:c.691T>C
|
ENSP00000245407.3:p.Ser231Pro
|
|
|
ENST00000415928.5:c.460T>C
|
ENSP00000388838.1:p.Ser154Pro
|
|
|
ENST00000435065.6:c.763T>C
|
ENSP00000402760.2:p.Ser255Pro
|
|
|
ENST00000437841.6:c.*6T>C
|
ENSP00000400553.1:n.*6T>C
|
|
|
ENST00000448810.5:c.39T>C
|
|
|
|
ENST00000461013.5:n.8113T>C
|
|
|
|
NM_001308122.1:c.763T>C
|
NP_001295051.1:p.Ser255Pro
|
|
|
NM_003060.3:c.691T>C
|
NP_003051.1:p.Ser231Pro
|
|
|
XM_011543590.1:c.73T>C
|
XP_011541892.1:p.Ser25Pro
|
|
|
XR_427718.1:n.1051T>C
|
|
|
|
XR_948290.1:n.1032T>C
|
|
|
|
XR_948291.1:n.1045T>C
|
|
|
|
XM_011543590.2:c.73T>C
|
XP_011541892.1:p.Ser25Pro
|
|
|
XM_017009778.2:c.163T>C
|
XP_016865267.1:p.Ser55Pro
|
|
|
XR_001742215.1:n.1032T>C
|
|
|
|
XR_001742216.1:n.1051T>C
|
|
|
|
XR_427718.2:n.1051T>C
|
|
|
|
XR_948290.2:n.1032T>C
|
|
|
|
XR_948291.2:n.1045T>C
|
|
|
|
NM_003060.4:c.691T>C
MANE Select
|
NP_003051.1:p.Ser231Pro
|
|
|
NM_001308122.2:c.763T>C
|
NP_001295051.1:p.Ser255Pro
|
|
