ENST00000355808.10:c.647A>C
|
ENSP00000348062.6:p.Asn216Thr
|
|
ENST00000379805.4:c.*318A>C
|
ENSP00000369133.3:n.*318A>C
|
|
ENST00000417819.6:c.710A>C
|
ENSP00000404616.2:p.Asn237Thr
|
|
ENST00000423505.6:c.740A>C
|
ENSP00000406473.2:p.Asn247Thr
|
|
ENST00000481733.2:n.421A>C
|
|
|
ENST00000696704.1:c.441A>C
|
ENSP00000512823.1:p.Gln147His
|
|
ENST00000696705.1:c.*81A>C
|
ENSP00000512824.1:n.*81A>C
|
|
ENST00000422285.7:c.626A>C
MANE Select
|
ENSP00000394382.2:p.Asn209Thr
|
|
ENST00000379806.9:c.740A>C
|
ENSP00000369134.5:p.Asn247Thr
|
|
ENST00000422285.6:c.626A>C
|
ENSP00000394382.2:p.Asn209Thr
|
|
ENST00000479146.1:n.461A>C
|
|
|
ENST00000481733.1:n.54A>C
|
|
|
ENST00000540249.5:c.533A>C
|
ENSP00000440761.1:p.Asn178Thr
|
|
ENST00000545074.5:c.647A>C
|
ENSP00000438550.1:p.Asn216Thr
|
|
NM_000284.3:c.626A>C
|
NP_000275.1:p.Asn209Thr
|
|
NM_001173454.1:c.740A>C
|
NP_001166925.1:p.Asn247Thr
|
|
NM_001173455.1:c.647A>C
|
NP_001166926.1:p.Asn216Thr
|
|
NM_001173456.1:c.533A>C
|
NP_001166927.1:p.Asn178Thr
|
|
XM_011545531.1:c.761A>C
|
XP_011543833.1:p.Asn254Thr
|
|
XM_011545532.1:c.668A>C
|
XP_011543834.1:p.Asn223Thr
|
|
XM_017029574.2:c.647A>C
|
XP_016885063.1:p.Asn216Thr
|
|
NM_000284.4:c.626A>C
MANE Select
|
NP_000275.1:p.Asn209Thr
|
|
NM_001173454.2:c.740A>C
|
NP_001166925.1:p.Asn247Thr
|
|
NM_001173455.2:c.647A>C
|
NP_001166926.1:p.Asn216Thr
|
|
NM_001173456.2:c.533A>C
|
NP_001166927.1:p.Asn178Thr
|
|