ENST00000415928.6:c.1196A>T
|
ENSP00000388838.2:p.Glu399Val
|
|
ENST00000435065.7:c.1427A>T
|
ENSP00000402760.2:p.Glu476Val
|
|
ENST00000448810.6:c.*207A>T
|
ENSP00000401860.2:n.*207A>T
|
|
ENST00000685543.1:n.1496A>T
|
|
|
ENST00000686757.1:c.*519A>T
|
ENSP00000510721.1:n.*519A>T
|
|
ENST00000687740.1:n.4040A>T
|
|
|
ENST00000688151.1:n.2665A>T
|
|
|
ENST00000689271.1:c.1202A>T
|
ENSP00000510797.1:p.Glu401Val
|
|
ENST00000690900.1:c.*519A>T
|
ENSP00000510703.1:n.*519A>T
|
|
ENST00000692212.1:n.4495A>T
|
|
|
ENST00000692355.1:c.608A>T
|
|
|
ENST00000692413.1:c.1337A>T
|
ENSP00000509374.1:p.Glu446Val
|
|
ENST00000692825.1:c.1423A>T
|
ENSP00000509447.1:n.1423A>T
|
|
ENST00000693308.1:c.1403A>T
|
ENSP00000509770.1:p.Glu468Val
|
|
ENST00000693763.1:n.2515A>T
|
|
|
ENST00000245407.8:c.1355A>T
MANE Select
|
ENSP00000245407.3:p.Glu452Val
|
|
ENST00000245407.7:c.1355A>T
|
ENSP00000245407.3:p.Glu452Val
|
|
ENST00000435065.6:c.1427A>T
|
ENSP00000402760.2:p.Glu476Val
|
|
ENST00000447841.5:c.199A>T
|
|
|
ENST00000448810.5:c.617A>T
|
|
|
ENST00000461013.5:n.8777A>T
|
|
|
ENST00000475308.1:n.2033A>T
|
|
|
ENST00000479605.5:n.458A>T
|
|
|
NM_001308122.1:c.1427A>T
|
NP_001295051.1:p.Glu476Val
|
|
NM_003060.3:c.1355A>T
|
NP_003051.1:p.Glu452Val
|
|
XM_011543590.1:c.737A>T
|
XP_011541892.1:p.Glu246Val
|
|
XR_948290.1:n.1481A>T
|
|
|
XM_011543590.2:c.737A>T
|
XP_011541892.1:p.Glu246Val
|
|
XM_017009778.2:c.827A>T
|
XP_016865267.1:p.Glu276Val
|
|
XR_001742215.1:n.1610A>T
|
|
|
XR_001742216.1:n.1629A>T
|
|
|
XR_427718.2:n.1715A>T
|
|
|
XR_948290.2:n.1481A>T
|
|
|
XR_948291.2:n.1709A>T
|
|
|
NM_003060.4:c.1355A>T
MANE Select
|
NP_003051.1:p.Glu452Val
|
|
NM_001308122.2:c.1427A>T
|
NP_001295051.1:p.Glu476Val
|
|