ENST00000343631.4:c.1061_1062insC
|
ENSP00000342656.3:p.Glu354AspfsTer4
|
|
ENST00000395673.8:c.1061_1062insC
|
ENSP00000379032.4:p.Glu354AspfsTer4
|
|
ENST00000531161.6:n.1220_1221insC
|
|
|
ENST00000682359.1:c.939+1953_939+1954insC
|
ENSP00000508226.1:n.939+1953_939+1954insC
|
|
ENST00000682711.1:c.-544+31085_-544+31086insC
|
ENSP00000506803.1:n.-544+31085_-544+31086insC
|
|
ENST00000682815.1:c.1061_1062insC
|
ENSP00000507234.1:p.Glu354AspfsTer4
|
|
ENST00000682947.1:n.1235_1236insC
|
|
|
ENST00000682993.1:c.1061_1062insC
|
ENSP00000507580.1:p.Glu354AspfsTer4
|
|
ENST00000683000.1:c.1061_1062insC
|
ENSP00000508361.1:p.Glu354AspfsTer4
|
|
ENST00000683299.1:n.1478_1479insC
|
|
|
ENST00000683870.1:c.1061_1062insC
|
ENSP00000507922.1:p.Glu354AspfsTer4
|
|
ENST00000683881.1:n.3622_3623insC
|
|
|
ENST00000684039.1:c.1061_1062insC
|
ENSP00000507677.1:p.Glu354AspfsTer4
|
|
ENST00000684124.1:c.1061_1062insC
|
ENSP00000508332.1:p.Glu354AspfsTer4
|
|
ENST00000684533.1:c.744-3108_744-3107insC
|
ENSP00000507915.1:n.744-3108_744-3107insC
|
|
ENST00000533608.7:c.1061_1062insC
MANE Select
|
ENSP00000431173.2:p.Glu354AspfsTer4
|
|
ENST00000343631.3:c.1061_1062insC
|
ENSP00000342656.3:p.Glu354AspfsTer4
|
|
ENST00000358681.8:c.1061_1062insC
|
ENSP00000351509.4:p.Glu354AspfsTer4
|
|
ENST00000395673.7:c.1160_1161insC
|
ENSP00000379032.3:p.Glu387AspfsTer4
|
|
ENST00000525559.1:n.35_36insC
|
|
|
ENST00000531161.5:n.238_239insC
|
|
|
ENST00000533608.5:c.1061_1062insC
|
ENSP00000431173.1:p.Glu354AspfsTer4
|
|
NM_000401.3:c.1160_1161insC , LRG_494t1:c.1160_1161insC
|
NP_000392.3:p.Glu387AspfsTer4
|
|
NM_001178083.1:c.1061_1062insC
|
NP_001171554.1:p.Glu354AspfsTer4
|
|
NM_207122.1:c.1061_1062insC , LRG_494t2:c.1061_1062insC
|
NP_997005.1:p.Glu354AspfsTer4
|
|
XM_011519950.1:c.1199_1200insC
|
XP_011518252.1:p.Glu400AspfsTer4
|
|
XM_011519951.1:c.1100_1101insC
|
XP_011518253.1:p.Glu367AspfsTer4
|
|
XM_024448383.1:c.1199_1200insC
|
XP_024304151.1:p.Glu400AspfsTer4
|
|
NM_001178083.2:c.1061_1062insC
|
NP_001171554.1:p.Glu354AspfsTer4
|
|
NM_207122.2:c.1061_1062insC
MANE Select
|
NP_997005.1:p.Glu354AspfsTer4
|
|
NM_001178083.3:c.1061_1062insC
|
NP_001171554.1:p.Glu354AspfsTer4
|
|
NM_001389628.1:c.1061_1062insC
|
NP_001376557.1:p.Glu354AspfsTer4
|
|
NM_001389630.1:c.1061_1062insC
|
NP_001376559.1:p.Glu354AspfsTer4
|
|