ENST00000355808.10:c.876G>T
|
ENSP00000348062.6:p.Gln292His
|
|
ENST00000379805.4:c.*547G>T
|
ENSP00000369133.3:n.*547G>T
|
|
ENST00000417819.6:c.939G>T
|
ENSP00000404616.2:p.Gln313His
|
|
ENST00000423505.6:c.969G>T
|
ENSP00000406473.2:p.Gln323His
|
|
ENST00000481733.2:n.650G>T
|
|
|
ENST00000696704.1:c.*187G>T
|
ENSP00000512823.1:n.*187G>T
|
|
ENST00000696705.1:c.*310G>T
|
ENSP00000512824.1:n.*310G>T
|
|
ENST00000422285.7:c.855G>T
MANE Select
|
ENSP00000394382.2:p.Gln285His
|
|
ENST00000379804.1:c.12G>T
|
ENSP00000369132.1:p.Gln4His
|
|
ENST00000379806.9:c.969G>T
|
ENSP00000369134.5:p.Gln323His
|
|
ENST00000422285.6:c.855G>T
|
ENSP00000394382.2:p.Gln285His
|
|
ENST00000478795.1:n.294G>T
|
|
|
ENST00000481733.1:n.283G>T
|
|
|
ENST00000540249.5:c.762G>T
|
ENSP00000440761.1:p.Gln254His
|
|
ENST00000545074.5:c.876G>T
|
ENSP00000438550.1:p.Gln292His
|
|
NM_000284.3:c.855G>T
|
NP_000275.1:p.Gln285His
|
|
NM_001173454.1:c.969G>T
|
NP_001166925.1:p.Gln323His
|
|
NM_001173455.1:c.876G>T
|
NP_001166926.1:p.Gln292His
|
|
NM_001173456.1:c.762G>T
|
NP_001166927.1:p.Gln254His
|
|
XM_011545531.1:c.990G>T
|
XP_011543833.1:p.Gln330His
|
|
XM_011545532.1:c.897G>T
|
XP_011543834.1:p.Gln299His
|
|
XM_017029574.2:c.876G>T
|
XP_016885063.1:p.Gln292His
|
|
NM_000284.4:c.855G>T
MANE Select
|
NP_000275.1:p.Gln285His
|
|
NM_001173454.2:c.969G>T
|
NP_001166925.1:p.Gln323His
|
|
NM_001173455.2:c.876G>T
|
NP_001166926.1:p.Gln292His
|
|
NM_001173456.2:c.762G>T
|
NP_001166927.1:p.Gln254His
|
|