ENST00000249750.9:c.377T>G
MANE Select
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ENSP00000249750.4:p.Leu126Arg
|
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ENST00000249750.8:c.377T>G
|
ENSP00000249750.4:p.Leu126Arg
|
|
ENST00000347587.7:c.377T>G
|
ENSP00000309623.3:p.Leu126Arg
|
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ENST00000430119.6:c.*351T>G
|
ENSP00000416754.2:n.*351T>G
|
|
ENST00000537372.5:c.314T>G
|
ENSP00000438296.1:p.Leu105Arg
|
|
ENST00000558231.5:c.290T>G
|
ENSP00000453600.1:p.Leu97Arg
|
|
ENST00000559266.5:n.318+3093T>G
|
|
|
ENST00000559517.5:c.89T>G
|
ENSP00000453408.1:p.Leu30Arg
|
|
ENST00000561070.5:c.89T>G
|
ENSP00000452850.1:p.Leu30Arg
|
|
NM_001206897.1:c.314T>G
|
NP_001193826.1:p.Leu105Arg
|
|
NM_003888.3:c.377T>G
|
NP_003879.2:p.Leu126Arg
|
|
NM_170696.2:c.377T>G
|
NP_733797.1:p.Leu126Arg
|
|
NM_170697.2:c.89T>G
|
NP_733798.1:p.Leu30Arg
|
|
XM_024450095.1:c.377T>G
|
XP_024305863.1:p.Leu126Arg
|
|
NM_003888.4:c.377T>G
MANE Select
|
NP_003879.2:p.Leu126Arg
|
|
NM_170696.3:c.377T>G
|
NP_733797.1:p.Leu126Arg
|
|
NM_170697.3:c.89T>G
|
NP_733798.1:p.Leu30Arg
|
|
NM_001206897.2:c.314T>G
|
NP_001193826.1:p.Leu105Arg
|
|