ENST00000355808.10:c.723G>C
|
ENSP00000348062.6:p.Glu241Asp
|
|
ENST00000379805.4:c.*394G>C
|
ENSP00000369133.3:n.*394G>C
|
|
ENST00000417819.6:c.786G>C
|
ENSP00000404616.2:p.Glu262Asp
|
|
ENST00000423505.6:c.816G>C
|
ENSP00000406473.2:p.Glu272Asp
|
|
ENST00000481733.2:n.497G>C
|
|
|
ENST00000696704.1:c.*34G>C
|
ENSP00000512823.1:n.*34G>C
|
|
ENST00000696705.1:c.*157G>C
|
ENSP00000512824.1:n.*157G>C
|
|
ENST00000422285.7:c.702G>C
MANE Select
|
ENSP00000394382.2:p.Glu234Asp
|
|
ENST00000379806.9:c.816G>C
|
ENSP00000369134.5:p.Glu272Asp
|
|
ENST00000422285.6:c.702G>C
|
ENSP00000394382.2:p.Glu234Asp
|
|
ENST00000481733.1:n.130G>C
|
|
|
ENST00000540249.5:c.609G>C
|
ENSP00000440761.1:p.Glu203Asp
|
|
ENST00000545074.5:c.723G>C
|
ENSP00000438550.1:p.Glu241Asp
|
|
NM_000284.3:c.702G>C
|
NP_000275.1:p.Glu234Asp
|
|
NM_001173454.1:c.816G>C
|
NP_001166925.1:p.Glu272Asp
|
|
NM_001173455.1:c.723G>C
|
NP_001166926.1:p.Glu241Asp
|
|
NM_001173456.1:c.609G>C
|
NP_001166927.1:p.Glu203Asp
|
|
XM_011545531.1:c.837G>C
|
XP_011543833.1:p.Glu279Asp
|
|
XM_011545532.1:c.744G>C
|
XP_011543834.1:p.Glu248Asp
|
|
XM_017029574.2:c.723G>C
|
XP_016885063.1:p.Glu241Asp
|
|
NM_000284.4:c.702G>C
MANE Select
|
NP_000275.1:p.Glu234Asp
|
|
NM_001173454.2:c.816G>C
|
NP_001166925.1:p.Glu272Asp
|
|
NM_001173455.2:c.723G>C
|
NP_001166926.1:p.Glu241Asp
|
|
NM_001173456.2:c.609G>C
|
NP_001166927.1:p.Glu203Asp
|
|