|
ENST00000415928.6:c.974T>C
|
ENSP00000388838.2:p.Leu325Pro
|
|
|
ENST00000435065.7:c.1205T>C
|
ENSP00000402760.2:p.Leu402Pro
|
|
|
ENST00000448810.6:c.1053-6T>C
|
ENSP00000401860.2:n.1053-6T>C
|
|
|
ENST00000685543.1:n.1274T>C
|
|
|
|
ENST00000686757.1:c.*297T>C
|
ENSP00000510721.1:n.*297T>C
|
|
|
ENST00000687740.1:n.3818T>C
|
|
|
|
ENST00000688151.1:n.2443T>C
|
|
|
|
ENST00000689271.1:c.980T>C
|
ENSP00000510797.1:p.Leu327Pro
|
|
|
ENST00000690900.1:c.*297T>C
|
ENSP00000510703.1:n.*297T>C
|
|
|
ENST00000692212.1:n.2745T>C
|
|
|
|
ENST00000692355.1:c.386T>C
|
|
|
|
ENST00000692413.1:c.1115T>C
|
ENSP00000509374.1:p.Leu372Pro
|
|
|
ENST00000692825.1:c.1201T>C
|
ENSP00000509447.1:n.1201T>C
|
|
|
ENST00000693308.1:c.1181T>C
|
ENSP00000509770.1:p.Leu394Pro
|
|
|
ENST00000693763.1:n.2293T>C
|
|
|
|
ENST00000245407.8:c.1133T>C
MANE Select
|
ENSP00000245407.3:p.Leu378Pro
|
|
|
ENST00000245407.7:c.1133T>C
|
ENSP00000245407.3:p.Leu378Pro
|
|
|
ENST00000435065.6:c.1205T>C
|
ENSP00000402760.2:p.Leu402Pro
|
|
|
ENST00000447841.5:c.112-1663T>C
|
|
|
|
ENST00000448810.5:c.401-6T>C
|
|
|
|
ENST00000461013.5:n.8555T>C
|
|
|
|
ENST00000475308.1:n.1811T>C
|
|
|
|
ENST00000479605.5:n.236T>C
|
|
|
|
NM_001308122.1:c.1205T>C
|
NP_001295051.1:p.Leu402Pro
|
|
|
NM_003060.3:c.1133T>C
|
NP_003051.1:p.Leu378Pro
|
|
|
XM_011543590.1:c.515T>C
|
XP_011541892.1:p.Leu172Pro
|
|
|
XR_427718.1:n.1493T>C
|
|
|
|
XR_948290.1:n.1394-1663T>C
|
|
|
|
XR_948291.1:n.1487T>C
|
|
|
|
XM_011543590.2:c.515T>C
|
XP_011541892.1:p.Leu172Pro
|
|
|
XM_017009778.2:c.605T>C
|
XP_016865267.1:p.Leu202Pro
|
|
|
XR_001742215.1:n.1394-6T>C
|
|
|
|
XR_001742216.1:n.1413-6T>C
|
|
|
|
XR_427718.2:n.1493T>C
|
|
|
|
XR_948290.2:n.1394-1663T>C
|
|
|
|
XR_948291.2:n.1487T>C
|
|
|
|
NM_003060.4:c.1133T>C
MANE Select
|
NP_003051.1:p.Leu378Pro
|
|
|
NM_001308122.2:c.1205T>C
|
NP_001295051.1:p.Leu402Pro
|
|
