|
ENST00000507116.6:c.394G>C
|
ENSP00000424852.1:p.Asp132His
|
|
|
ENST00000340635.11:c.586G>C
MANE Select
|
ENSP00000345502.6:p.Asp196His
|
|
|
ENST00000636120.1:c.256G>C
|
ENSP00000490821.1:p.Asp86His
|
|
|
ENST00000638939.1:c.151G>C
|
ENSP00000492052.1:p.Asp51His
|
|
|
ENST00000309641.10:c.394G>C
|
ENSP00000308485.6:p.Asp132His
|
|
|
ENST00000340635.10:c.586G>C
|
ENSP00000345502.6:p.Asp196His
|
|
|
ENST00000360047.9:c.178G>C
|
ENSP00000353152.5:p.Asp60His
|
|
|
ENST00000405053.7:n.249G>C
|
|
|
|
ENST00000405755.6:c.220G>C
|
ENSP00000384806.2:p.Asp74His
|
|
|
ENST00000502484.6:c.403G>C
|
ENSP00000423094.2:p.Asp135His
|
|
|
ENST00000502575.1:c.394G>C
|
ENSP00000425917.1:p.Asp132His
|
|
|
ENST00000503258.5:c.196G>C
|
ENSP00000425605.1:p.Asp66His
|
|
|
ENST00000505453.1:c.-98-176867G>C
|
ENSP00000421013.1:n.-98-176867G>C
|
|
|
ENST00000507116.5:c.394G>C
|
ENSP00000424852.1:p.Asp132His
|
|
|
ENST00000514231.1:n.349G>C
|
|
|
|
ENST00000515324.1:n.98G>C
|
|
|
|
ENST00000546160.5:c.193G>C
|
ENSP00000442734.2:p.Asp65His
|
|
|
ENST00000621323.4:n.131G>C
|
|
|
|
NM_001104631.1:c.586G>C
|
NP_001098101.1:p.Asp196His
|
|
|
NM_001165899.1:c.403G>C
|
NP_001159371.1:p.Asp135His
|
|
|
NM_001197218.1:c.394G>C
|
NP_001184147.1:p.Asp132His
|
|
|
NM_001197219.1:c.220G>C
|
NP_001184148.1:p.Asp74His
|
|
|
NM_001197220.1:c.196G>C
|
NP_001184149.1:p.Asp66His
|
|
|
NM_006203.4:c.178G>C
|
NP_006194.2:p.Asp60His
|
|
|
XM_005248537.2:c.256G>C
|
XP_005248594.1:p.Asp86His
|
|
|
XM_005248538.3:c.178G>C
|
XP_005248595.1:p.Asp60His
|
|
|
XM_011543469.1:c.550G>C
|
XP_011541771.1:p.Asp184His
|
|
|
XM_011543470.1:c.550G>C
|
XP_011541772.1:p.Asp184His
|
|
|
XM_011543471.1:c.403G>C
|
XP_011541773.1:p.Asp135His
|
|
|
XM_011543472.1:c.403G>C
|
XP_011541774.1:p.Asp135His
|
|
|
XM_011543473.1:c.403G>C
|
XP_011541775.1:p.Asp135His
|
|
|
XM_011543474.1:c.373G>C
|
XP_011541776.1:p.Asp125His
|
|
|
XM_011543475.1:c.220G>C
|
XP_011541777.1:p.Asp74His
|
|
|
XM_011543476.1:c.166G>C
|
XP_011541778.1:p.Asp56His
|
|
|
XM_011543477.1:c.145G>C
|
XP_011541779.1:p.Asp49His
|
|
|
XM_011543478.1:c.82G>C
|
XP_011541780.1:p.Asp28His
|
|
|
XM_011543479.1:c.82G>C
|
XP_011541781.1:p.Asp28His
|
|
|
NM_001349241.1:c.373G>C
|
NP_001336170.1:p.Asp125His
|
|
|
NM_001349242.1:c.256G>C
|
NP_001336171.1:p.Asp86His
|
|
|
NM_001349243.1:c.-109G>C
|
NP_001336172.1:n.-109G>C
|
|
|
NM_001364599.1:c.403G>C
|
NP_001351528.1:p.Asp135His
|
|
|
NM_001364600.1:c.403G>C
|
NP_001351529.1:p.Asp135His
|
|
|
NM_001364601.1:c.394G>C
|
NP_001351530.1:p.Asp132His
|
|
|
NM_001364602.1:c.394G>C
|
NP_001351531.1:p.Asp132His
|
|
|
NM_001364603.1:c.-365G>C
|
NP_001351532.1:n.-365G>C
|
|
|
NM_001364604.1:c.-109G>C
|
NP_001351533.1:n.-109G>C
|
|
|
XM_011543470.2:c.550G>C
|
XP_011541772.1:p.Asp184His
|
|
|
XM_011543471.2:c.403G>C
|
XP_011541773.1:p.Asp135His
|
|
|
XM_017009565.1:c.550G>C
|
XP_016865054.1:p.Asp184His
|
|
|
XM_017009566.1:c.403G>C
|
XP_016865055.1:p.Asp135His
|
|
|
XM_017009567.1:c.388G>C
|
XP_016865056.1:p.Asp130His
|
|
|
XM_024446110.1:c.550G>C
|
XP_024301878.1:p.Asp184His
|
|
|
XM_024446112.1:c.403G>C
|
XP_024301880.1:p.Asp135His
|
|
|
NM_001104631.2:c.586G>C
MANE Select
|
NP_001098101.1:p.Asp196His
|
|
|
NM_001165899.2:c.403G>C
|
NP_001159371.1:p.Asp135His
|
|
|
NM_001197218.2:c.394G>C
|
NP_001184147.1:p.Asp132His
|
|
|
NM_001197219.2:c.220G>C
|
NP_001184148.1:p.Asp74His
|
|
|
NM_001197220.2:c.196G>C
|
NP_001184149.1:p.Asp66His
|
|
|
NM_001349241.2:c.373G>C
|
NP_001336170.1:p.Asp125His
|
|
|
NM_001349243.2:c.-109G>C
|
NP_001336172.1:n.-109G>C
|
|
|
NM_001364600.2:c.403G>C
|
NP_001351529.1:p.Asp135His
|
|
|
NM_001364602.2:c.394G>C
|
NP_001351531.1:p.Asp132His
|
|
|
NM_001349242.2:c.256G>C
|
NP_001336171.1:p.Asp86His
|
|
|
NM_006203.5:c.178G>C
|
NP_006194.2:p.Asp60His
|
|
