|
NM_021625.5:c.1465G>A
MANE Select
|
NP_067638.3:p.Ala489Thr
|
|
ENST00000261740.7:c.1465G>A
MANE Select
|
ENSP00000261740.2:p.Ala489Thr
|
|
NM_001177428.1:c.1324G>A
|
NP_001170899.1:p.Ala442Thr
|
|
NM_001177431.1:c.1363G>A
|
NP_001170902.1:p.Ala455Thr
|
|
NM_001177433.1:c.1144G>A
|
NP_001170904.1:p.Ala382Thr
|
|
NM_021625.4:c.1465G>A , LRG_372t1:c.1465G>A
|
NP_067638.3:p.Ala489Thr
|
|
NM_147204.2:c.1285G>A
|
NP_671737.1:p.Ala429Thr
|
|
ENST00000261740.6:c.1465G>A
|
ENSP00000261740.2:p.Ala489Thr
|
|
ENST00000418703.6:c.1465G>A
|
ENSP00000406191.2:p.Ala489Thr
|
|
ENST00000418703.7:c.1465G>A
|
ENSP00000406191.2:p.Ala489Thr
|
|
ENST00000536838.1:c.1363G>A
|
ENSP00000444336.1:p.Ala455Thr
|
|
ENST00000537083.5:c.1285G>A
|
ENSP00000442738.1:p.Ala429Thr
|
|
ENST00000538125.5:c.1465G>A
|
ENSP00000437449.1:p.Ala489Thr
|
|
ENST00000541794.5:c.1324G>A
|
ENSP00000442167.1:p.Ala442Thr
|
|
ENST00000544971.5:c.1144G>A
|
ENSP00000443611.1:p.Ala382Thr
|
|
ENST00000674908.1:c.*552G>A
|
ENSP00000502012.1:n.*552G>A
|
|
ENST00000675533.1:n.1496G>A
|
|
|
ENST00000675670.1:c.1465G>A
|
ENSP00000502135.1:p.Ala489Thr
|
|
ENST00000676376.1:n.1496G>A
|
|
|
XM_005253918.1:c.1465G>A
|
XP_005253975.1:p.Ala489Thr
|
|
XM_011538630.1:c.1465G>A
|
XP_011536932.1:p.Ala489Thr
|
|
XM_011538630.2:c.1618G>A
|
XP_011536932.2:p.Ala540Thr
|
|
XM_011538631.1:c.1324G>A
|
XP_011536933.1:p.Ala442Thr
|
|
XM_011538631.2:c.1477G>A
|
XP_011536933.2:p.Ala493Thr
|
|
XM_011538632.1:c.1285G>A
|
XP_011536934.1:p.Ala429Thr
|
|
XM_011538632.2:c.1438G>A
|
XP_011536934.2:p.Ala480Thr
|
|
XM_011538633.1:c.1144G>A
|
XP_011536935.1:p.Ala382Thr
|
|
XM_011538633.2:c.1297G>A
|
XP_011536935.2:p.Ala433Thr
|
|
XM_011538634.1:c.1465G>A
|
XP_011536936.1:p.Ala489Thr
|
|
XM_011538634.2:c.1618G>A
|
XP_011536936.2:p.Ala540Thr
|
|
XM_011538635.1:c.1618G>A
|
XP_011536937.1:p.Ala540Thr
|
|
XM_011538635.2:c.1618G>A
|
XP_011536937.1:p.Ala540Thr
|
|
XM_011538636.1:c.1618G>A
|
XP_011536938.1:p.Ala540Thr
|
|
XM_017019774.1:c.1465G>A
|
XP_016875263.1:p.Ala489Thr
|
