ENST00000355808.10:c.679T>A
|
ENSP00000348062.6:p.Phe227Ile
|
|
ENST00000379805.4:c.*350T>A
|
ENSP00000369133.3:n.*350T>A
|
|
ENST00000417819.6:c.742T>A
|
ENSP00000404616.2:p.Phe248Ile
|
|
ENST00000423505.6:c.772T>A
|
ENSP00000406473.2:p.Phe258Ile
|
|
ENST00000481733.2:n.453T>A
|
|
|
ENST00000696704.1:c.473T>A
|
ENSP00000512823.1:p.Phe158Tyr
|
|
ENST00000696705.1:c.*113T>A
|
ENSP00000512824.1:n.*113T>A
|
|
ENST00000422285.7:c.658T>A
MANE Select
|
ENSP00000394382.2:p.Phe220Ile
|
|
ENST00000379806.9:c.772T>A
|
ENSP00000369134.5:p.Phe258Ile
|
|
ENST00000422285.6:c.658T>A
|
ENSP00000394382.2:p.Phe220Ile
|
|
ENST00000479146.1:n.493T>A
|
|
|
ENST00000481733.1:n.86T>A
|
|
|
ENST00000540249.5:c.565T>A
|
ENSP00000440761.1:p.Phe189Ile
|
|
ENST00000545074.5:c.679T>A
|
ENSP00000438550.1:p.Phe227Ile
|
|
NM_000284.3:c.658T>A
|
NP_000275.1:p.Phe220Ile
|
|
NM_001173454.1:c.772T>A
|
NP_001166925.1:p.Phe258Ile
|
|
NM_001173455.1:c.679T>A
|
NP_001166926.1:p.Phe227Ile
|
|
NM_001173456.1:c.565T>A
|
NP_001166927.1:p.Phe189Ile
|
|
XM_011545531.1:c.793T>A
|
XP_011543833.1:p.Phe265Ile
|
|
XM_011545532.1:c.700T>A
|
XP_011543834.1:p.Phe234Ile
|
|
XM_017029574.2:c.679T>A
|
XP_016885063.1:p.Phe227Ile
|
|
NM_000284.4:c.658T>A
MANE Select
|
NP_000275.1:p.Phe220Ile
|
|
NM_001173454.2:c.772T>A
|
NP_001166925.1:p.Phe258Ile
|
|
NM_001173455.2:c.679T>A
|
NP_001166926.1:p.Phe227Ile
|
|
NM_001173456.2:c.565T>A
|
NP_001166927.1:p.Phe189Ile
|
|