ENST00000230771.9:c.546G>C
MANE Select
|
ENSP00000230771.3:p.Gln182His
|
|
ENST00000503873.6:c.324G>C
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ENSP00000424516.2:p.Gln108His
|
|
ENST00000509299.6:c.336G>C
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ENSP00000425695.2:p.Gln112His
|
|
ENST00000520095.6:c.*124G>C
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ENSP00000429220.1:n.*124G>C
|
|
ENST00000642452.1:c.512G>C
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|
|
ENST00000642752.1:c.546G>C
|
ENSP00000493630.1:p.Gln182His
|
|
ENST00000642970.1:c.336G>C
|
ENSP00000496011.1:p.Gln112His
|
|
ENST00000643996.1:c.336G>C
|
ENSP00000495350.1:p.Gln112His
|
|
ENST00000645065.1:c.564G>C
|
ENSP00000493571.1:p.Gln188His
|
|
ENST00000645749.1:c.546G>C
|
ENSP00000494296.1:p.Gln182His
|
|
ENST00000646468.1:c.564G>C
|
ENSP00000494965.1:p.Gln188His
|
|
ENST00000647484.1:c.336G>C
|
ENSP00000494140.1:p.Gln112His
|
|
ENST00000230771.7:c.546G>C
|
ENSP00000230771.3:p.Gln182His
|
|
ENST00000448069.2:c.129G>C
|
ENSP00000407105.2:p.Gln43His
|
|
ENST00000508522.5:c.471G>C
|
ENSP00000423616.1:p.Gln157His
|
|
ENST00000510104.5:c.*346G>C
|
ENSP00000423530.1:n.*346G>C
|
|
ENST00000513688.1:n.553G>C
|
|
|
ENST00000520095.5:c.*124G>C
|
ENSP00000429220.1:n.*124G>C
|
|
NM_001278731.1:c.471G>C
|
NP_001265660.1:p.Gln157His
|
|
NM_001278732.1:c.114G>C
|
NP_001265661.1:p.Gln38His
|
|
NM_012208.3:c.546G>C
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NP_036340.1:p.Gln182His
|
|
XM_011537619.1:c.564G>C
|
XP_011535921.1:p.Gln188His
|
|
XM_011537620.1:c.564G>C
|
XP_011535922.1:p.Gln188His
|
|
NM_001363535.1:c.564G>C
|
NP_001350464.1:p.Gln188His
|
|
NM_001363536.1:c.336G>C
|
NP_001350465.1:p.Gln112His
|
|
XM_017009288.1:c.336G>C
|
XP_016864777.1:p.Gln112His
|
|
XM_017009289.1:c.336G>C
|
XP_016864778.1:p.Gln112His
|
|
XM_017009290.2:c.-189G>C
|
XP_016864779.1:n.-189G>C
|
|
XM_017009291.1:c.-189G>C
|
XP_016864780.1:n.-189G>C
|
|
XM_017009292.1:c.-189G>C
|
XP_016864781.1:n.-189G>C
|
|
NM_012208.4:c.546G>C
MANE Select
|
NP_036340.1:p.Gln182His
|
|
NM_001278731.2:c.471G>C
|
NP_001265660.1:p.Gln157His
|
|
NM_001278732.2:c.114G>C
|
NP_001265661.1:p.Gln38His
|
|
NM_001363535.2:c.564G>C
|
NP_001350464.1:p.Gln188His
|
|
NM_001363536.2:c.336G>C
|
NP_001350465.1:p.Gln112His
|
|