ENST00000347454.9:c.692G>A
MANE Select
|
ENSP00000233552.6:p.Arg231His
|
|
ENST00000347454.8:c.692G>A
|
ENSP00000233552.5:p.Arg231His
|
|
ENST00000405940.6:c.666G>A
|
ENSP00000384375.2:p.Ser222=
|
|
ENST00000417567.1:c.268G>A
|
|
|
ENST00000445933.6:c.689G>A
|
ENSP00000394397.2:p.Arg230His
|
|
ENST00000451130.6:c.752G>A
|
ENSP00000394869.2:p.Arg251His
|
|
ENST00000475582.5:n.1813G>A
|
|
|
ENST00000493344.6:c.755G>A
|
ENSP00000429323.1:p.Arg252His
|
|
ENST00000616081.4:c.683G>A
|
ENSP00000477710.1:p.Arg228His
|
|
ENST00000622434.4:c.647G>A
|
ENSP00000479991.1:p.Arg216His
|
|
NM_001034116.1:c.692G>A
|
NP_001029288.1:p.Arg231His
|
|
NM_015636.3:c.689G>A
|
NP_056451.3:p.Arg230His
|
|
NM_172195.3:c.752G>A
|
NP_751945.2:p.Arg251His
|
|
XM_005264632.1:c.647G>A
|
XP_005264689.1:p.Arg216His
|
|
XM_006712132.1:c.644G>A
|
XP_006712195.1:p.Arg215His
|
|
XM_011533147.1:c.74G>A
|
XP_011531449.1:p.Arg25His
|
|
NM_001318965.1:c.755G>A
|
NP_001305894.1:p.Arg252His
|
|
NM_001318966.1:c.647G>A
|
NP_001305895.1:p.Arg216His
|
|
NM_001318967.1:c.599G>A
|
NP_001305896.1:p.Arg200His
|
|
NM_001318968.1:c.107G>A
|
NP_001305897.1:p.Arg36His
|
|
NM_001318969.1:c.74G>A
|
NP_001305898.1:p.Arg25His
|
|
XM_011533147.2:c.74G>A
|
XP_011531449.1:p.Arg25His
|
|
NM_001034116.2:c.692G>A
MANE Select
|
NP_001029288.1:p.Arg231His
|
|
NM_001318965.2:c.755G>A
|
NP_001305894.1:p.Arg252His
|
|
NM_001318966.2:c.647G>A
|
NP_001305895.1:p.Arg216His
|
|
NM_001318967.2:c.599G>A
|
NP_001305896.1:p.Arg200His
|
|
NM_001318968.2:c.107G>A
|
NP_001305897.1:p.Arg36His
|
|
NM_001318969.2:c.74G>A
|
NP_001305898.1:p.Arg25His
|
|
NM_015636.4:c.689G>A
|
NP_056451.3:p.Arg230His
|
|
NM_172195.4:c.752G>A
|
NP_751945.2:p.Arg251His
|
|