ENST00000415928.6:c.917T>C
|
ENSP00000388838.2:p.Phe306Ser
|
|
ENST00000435065.7:c.1148T>C
|
ENSP00000402760.2:p.Phe383Ser
|
|
ENST00000448810.6:c.1053-63T>C
|
ENSP00000401860.2:n.1053-63T>C
|
|
ENST00000685543.1:n.1217T>C
|
|
|
ENST00000686757.1:c.*240T>C
|
ENSP00000510721.1:n.*240T>C
|
|
ENST00000687740.1:n.3761T>C
|
|
|
ENST00000688151.1:n.2386T>C
|
|
|
ENST00000689271.1:c.923T>C
|
ENSP00000510797.1:p.Phe308Ser
|
|
ENST00000690900.1:c.*240T>C
|
ENSP00000510703.1:n.*240T>C
|
|
ENST00000692212.1:n.2688T>C
|
|
|
ENST00000692355.1:c.329T>C
|
|
|
ENST00000692413.1:c.1058T>C
|
ENSP00000509374.1:p.Phe353Ser
|
|
ENST00000692825.1:c.1144T>C
|
ENSP00000509447.1:n.1144T>C
|
|
ENST00000693308.1:c.1124T>C
|
ENSP00000509770.1:p.Phe375Ser
|
|
ENST00000693763.1:n.2236T>C
|
|
|
ENST00000245407.8:c.1076T>C
MANE Select
|
ENSP00000245407.3:p.Phe359Ser
|
|
ENST00000245407.7:c.1076T>C
|
ENSP00000245407.3:p.Phe359Ser
|
|
ENST00000435065.6:c.1148T>C
|
ENSP00000402760.2:p.Phe383Ser
|
|
ENST00000447841.5:c.111+1692T>C
|
|
|
ENST00000448810.5:c.401-63T>C
|
|
|
ENST00000461013.5:n.8498T>C
|
|
|
ENST00000475308.1:n.1754T>C
|
|
|
ENST00000479605.5:n.179T>C
|
|
|
NM_001308122.1:c.1148T>C
|
NP_001295051.1:p.Phe383Ser
|
|
NM_003060.3:c.1076T>C
|
NP_003051.1:p.Phe359Ser
|
|
XM_011543590.1:c.458T>C
|
XP_011541892.1:p.Phe153Ser
|
|
XR_427718.1:n.1436T>C
|
|
|
XR_948290.1:n.1393+1692T>C
|
|
|
XR_948291.1:n.1430T>C
|
|
|
XM_011543590.2:c.458T>C
|
XP_011541892.1:p.Phe153Ser
|
|
XM_017009778.2:c.548T>C
|
XP_016865267.1:p.Phe183Ser
|
|
XR_001742215.1:n.1394-63T>C
|
|
|
XR_001742216.1:n.1413-63T>C
|
|
|
XR_427718.2:n.1436T>C
|
|
|
XR_948290.2:n.1393+1692T>C
|
|
|
XR_948291.2:n.1430T>C
|
|
|
NM_003060.4:c.1076T>C
MANE Select
|
NP_003051.1:p.Phe359Ser
|
|
NM_001308122.2:c.1148T>C
|
NP_001295051.1:p.Phe383Ser
|
|