ENST00000355808.10:c.652G>A
|
ENSP00000348062.6:p.Ala218Thr
|
|
ENST00000379805.4:c.*323G>A
|
ENSP00000369133.3:n.*323G>A
|
|
ENST00000417819.6:c.715G>A
|
ENSP00000404616.2:p.Ala239Thr
|
|
ENST00000423505.6:c.745G>A
|
ENSP00000406473.2:p.Ala249Thr
|
|
ENST00000481733.2:n.426G>A
|
|
|
ENST00000696704.1:c.446G>A
|
ENSP00000512823.1:p.Gly149Asp
|
|
ENST00000696705.1:c.*86G>A
|
ENSP00000512824.1:n.*86G>A
|
|
ENST00000422285.7:c.631G>A
MANE Select
|
ENSP00000394382.2:p.Ala211Thr
|
|
ENST00000379806.9:c.745G>A
|
ENSP00000369134.5:p.Ala249Thr
|
|
ENST00000422285.6:c.631G>A
|
ENSP00000394382.2:p.Ala211Thr
|
|
ENST00000479146.1:n.466G>A
|
|
|
ENST00000481733.1:n.59G>A
|
|
|
ENST00000540249.5:c.538G>A
|
ENSP00000440761.1:p.Ala180Thr
|
|
ENST00000545074.5:c.652G>A
|
ENSP00000438550.1:p.Ala218Thr
|
|
NM_000284.3:c.631G>A
|
NP_000275.1:p.Ala211Thr
|
|
NM_001173454.1:c.745G>A
|
NP_001166925.1:p.Ala249Thr
|
|
NM_001173455.1:c.652G>A
|
NP_001166926.1:p.Ala218Thr
|
|
NM_001173456.1:c.538G>A
|
NP_001166927.1:p.Ala180Thr
|
|
XM_011545531.1:c.766G>A
|
XP_011543833.1:p.Ala256Thr
|
|
XM_011545532.1:c.673G>A
|
XP_011543834.1:p.Ala225Thr
|
|
XM_017029574.2:c.652G>A
|
XP_016885063.1:p.Ala218Thr
|
|
NM_000284.4:c.631G>A
MANE Select
|
NP_000275.1:p.Ala211Thr
|
|
NM_001173454.2:c.745G>A
|
NP_001166925.1:p.Ala249Thr
|
|
NM_001173455.2:c.652G>A
|
NP_001166926.1:p.Ala218Thr
|
|
NM_001173456.2:c.538G>A
|
NP_001166927.1:p.Ala180Thr
|
|