ENST00000257863.9:c.176G>A
MANE Select
|
ENSP00000257863.3:p.Arg59His
|
|
ENST00000257863.8:c.176G>A
|
ENSP00000257863.3:p.Arg59His
|
|
ENST00000379791.7:c.176G>A
|
ENSP00000369117.3:p.Arg59His
|
|
ENST00000550311.5:c.176G>A
|
ENSP00000446661.1:p.Arg59His
|
|
ENST00000553037.1:n.137G>A
|
|
|
NM_001164690.1:c.176G>A
|
NP_001158162.1:p.Arg59His
|
|
NM_001164691.1:c.176G>A
|
NP_001158163.1:p.Arg59His
|
|
NM_020547.2:c.176G>A
|
NP_065434.1:p.Arg59His
|
|
XM_011538173.1:c.176G>A
|
XP_011536475.1:p.Arg59His
|
|
XM_011538174.1:c.176G>A
|
XP_011536476.1:p.Arg59His
|
|
XM_011538175.1:c.176G>A
|
XP_011536477.1:p.Arg59His
|
|
XM_011538176.1:c.176G>A
|
XP_011536478.1:p.Arg59His
|
|
XM_011538177.1:c.176G>A
|
XP_011536479.1:p.Arg59His
|
|
XM_011538178.1:c.176G>A
|
XP_011536480.1:p.Arg59His
|
|
XM_011538179.1:c.176G>A
|
XP_011536481.1:p.Arg59His
|
|
XM_011538180.1:c.-72G>A
|
XP_011536482.1:n.-72G>A
|
|
XM_011538181.1:c.-72G>A
|
XP_011536483.1:n.-72G>A
|
|
XM_011538182.1:c.-72G>A
|
XP_011536484.1:n.-72G>A
|
|
XM_011538183.1:c.176G>A
|
XP_011536485.1:p.Arg59His
|
|
XM_011538184.1:c.176G>A
|
XP_011536486.1:p.Arg59His
|
|
XM_011538185.1:c.176G>A
|
XP_011536487.1:p.Arg59His
|
|
XM_011538187.1:c.176G>A
|
XP_011536489.1:p.Arg59His
|
|
NM_001164690.2:c.176G>A
|
NP_001158162.1:p.Arg59His
|
|
NM_001164691.2:c.176G>A
|
NP_001158163.1:p.Arg59His
|
|
NM_020547.3:c.176G>A
MANE Select
|
NP_065434.1:p.Arg59His
|
|
XM_011538183.2:c.176G>A
|
XP_011536485.1:p.Arg59His
|
|
XM_011538184.2:c.176G>A
|
XP_011536486.1:p.Arg59His
|
|
XM_017019179.2:c.176G>A
|
XP_016874668.1:p.Arg59His
|
|
XM_024448938.1:c.176G>A
|
XP_024304706.1:p.Arg59His
|
|
XR_002957309.1:n.256G>A
|
|
|
XR_002957310.1:n.256G>A
|
|
|
XR_002957311.1:n.256G>A
|
|
|
XR_002957312.1:n.256G>A
|
|
|