ENST00000355808.10:c.677T>A
|
ENSP00000348062.6:p.Ile226Asn
|
|
ENST00000379805.4:c.*348T>A
|
ENSP00000369133.3:n.*348T>A
|
|
ENST00000417819.6:c.740T>A
|
ENSP00000404616.2:p.Ile247Asn
|
|
ENST00000423505.6:c.770T>A
|
ENSP00000406473.2:p.Ile257Asn
|
|
ENST00000481733.2:n.451T>A
|
|
|
ENST00000696704.1:c.471T>A
|
ENSP00000512823.1:p.Tyr157Ter
|
|
ENST00000696705.1:c.*111T>A
|
ENSP00000512824.1:n.*111T>A
|
|
ENST00000422285.7:c.656T>A
MANE Select
|
ENSP00000394382.2:p.Ile219Asn
|
|
ENST00000379806.9:c.770T>A
|
ENSP00000369134.5:p.Ile257Asn
|
|
ENST00000422285.6:c.656T>A
|
ENSP00000394382.2:p.Ile219Asn
|
|
ENST00000479146.1:n.491T>A
|
|
|
ENST00000481733.1:n.84T>A
|
|
|
ENST00000540249.5:c.563T>A
|
ENSP00000440761.1:p.Ile188Asn
|
|
ENST00000545074.5:c.677T>A
|
ENSP00000438550.1:p.Ile226Asn
|
|
NM_000284.3:c.656T>A
|
NP_000275.1:p.Ile219Asn
|
|
NM_001173454.1:c.770T>A
|
NP_001166925.1:p.Ile257Asn
|
|
NM_001173455.1:c.677T>A
|
NP_001166926.1:p.Ile226Asn
|
|
NM_001173456.1:c.563T>A
|
NP_001166927.1:p.Ile188Asn
|
|
XM_011545531.1:c.791T>A
|
XP_011543833.1:p.Ile264Asn
|
|
XM_011545532.1:c.698T>A
|
XP_011543834.1:p.Ile233Asn
|
|
XM_017029574.2:c.677T>A
|
XP_016885063.1:p.Ile226Asn
|
|
NM_000284.4:c.656T>A
MANE Select
|
NP_000275.1:p.Ile219Asn
|
|
NM_001173454.2:c.770T>A
|
NP_001166925.1:p.Ile257Asn
|
|
NM_001173455.2:c.677T>A
|
NP_001166926.1:p.Ile226Asn
|
|
NM_001173456.2:c.563T>A
|
NP_001166927.1:p.Ile188Asn
|
|