ENST00000355808.10:c.779G>A
|
ENSP00000348062.6:p.Arg260Lys
|
|
ENST00000379805.4:c.*450G>A
|
ENSP00000369133.3:n.*450G>A
|
|
ENST00000417819.6:c.842G>A
|
ENSP00000404616.2:p.Arg281Lys
|
|
ENST00000423505.6:c.872G>A
|
ENSP00000406473.2:p.Arg291Lys
|
|
ENST00000481733.2:n.553G>A
|
|
|
ENST00000696704.1:c.*90G>A
|
ENSP00000512823.1:n.*90G>A
|
|
ENST00000696705.1:c.*213G>A
|
ENSP00000512824.1:n.*213G>A
|
|
ENST00000422285.7:c.758G>A
MANE Select
|
ENSP00000394382.2:p.Arg253Lys
|
|
ENST00000379806.9:c.872G>A
|
ENSP00000369134.5:p.Arg291Lys
|
|
ENST00000422285.6:c.758G>A
|
ENSP00000394382.2:p.Arg253Lys
|
|
ENST00000481733.1:n.186G>A
|
|
|
ENST00000540249.5:c.665G>A
|
ENSP00000440761.1:p.Arg222Lys
|
|
ENST00000545074.5:c.779G>A
|
ENSP00000438550.1:p.Arg260Lys
|
|
NM_000284.3:c.758G>A
|
NP_000275.1:p.Arg253Lys
|
|
NM_001173454.1:c.872G>A
|
NP_001166925.1:p.Arg291Lys
|
|
NM_001173455.1:c.779G>A
|
NP_001166926.1:p.Arg260Lys
|
|
NM_001173456.1:c.665G>A
|
NP_001166927.1:p.Arg222Lys
|
|
XM_011545531.1:c.893G>A
|
XP_011543833.1:p.Arg298Lys
|
|
XM_011545532.1:c.800G>A
|
XP_011543834.1:p.Arg267Lys
|
|
XM_017029574.2:c.779G>A
|
XP_016885063.1:p.Arg260Lys
|
|
NM_000284.4:c.758G>A
MANE Select
|
NP_000275.1:p.Arg253Lys
|
|
NM_001173454.2:c.872G>A
|
NP_001166925.1:p.Arg291Lys
|
|
NM_001173455.2:c.779G>A
|
NP_001166926.1:p.Arg260Lys
|
|
NM_001173456.2:c.665G>A
|
NP_001166927.1:p.Arg222Lys
|
|