ENST00000355808.10:c.742G>C
|
ENSP00000348062.6:p.Asp248His
|
|
ENST00000379805.4:c.*413G>C
|
ENSP00000369133.3:n.*413G>C
|
|
ENST00000417819.6:c.805G>C
|
ENSP00000404616.2:p.Asp269His
|
|
ENST00000423505.6:c.835G>C
|
ENSP00000406473.2:p.Asp279His
|
|
ENST00000481733.2:n.516G>C
|
|
|
ENST00000696704.1:c.*53G>C
|
ENSP00000512823.1:n.*53G>C
|
|
ENST00000696705.1:c.*176G>C
|
ENSP00000512824.1:n.*176G>C
|
|
ENST00000422285.7:c.721G>C
MANE Select
|
ENSP00000394382.2:p.Asp241His
|
|
ENST00000379806.9:c.835G>C
|
ENSP00000369134.5:p.Asp279His
|
|
ENST00000422285.6:c.721G>C
|
ENSP00000394382.2:p.Asp241His
|
|
ENST00000481733.1:n.149G>C
|
|
|
ENST00000540249.5:c.628G>C
|
ENSP00000440761.1:p.Asp210His
|
|
ENST00000545074.5:c.742G>C
|
ENSP00000438550.1:p.Asp248His
|
|
NM_000284.3:c.721G>C
|
NP_000275.1:p.Asp241His
|
|
NM_001173454.1:c.835G>C
|
NP_001166925.1:p.Asp279His
|
|
NM_001173455.1:c.742G>C
|
NP_001166926.1:p.Asp248His
|
|
NM_001173456.1:c.628G>C
|
NP_001166927.1:p.Asp210His
|
|
XM_011545531.1:c.856G>C
|
XP_011543833.1:p.Asp286His
|
|
XM_011545532.1:c.763G>C
|
XP_011543834.1:p.Asp255His
|
|
XM_017029574.2:c.742G>C
|
XP_016885063.1:p.Asp248His
|
|
NM_000284.4:c.721G>C
MANE Select
|
NP_000275.1:p.Asp241His
|
|
NM_001173454.2:c.835G>C
|
NP_001166925.1:p.Asp279His
|
|
NM_001173455.2:c.742G>C
|
NP_001166926.1:p.Asp248His
|
|
NM_001173456.2:c.628G>C
|
NP_001166927.1:p.Asp210His
|
|