ENST00000249750.9:c.370G>T
MANE Select
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ENSP00000249750.4:p.Glu124Ter
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ENST00000249750.8:c.370G>T
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ENSP00000249750.4:p.Glu124Ter
|
|
ENST00000347587.7:c.370G>T
|
ENSP00000309623.3:p.Glu124Ter
|
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ENST00000430119.6:c.*344G>T
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ENSP00000416754.2:n.*344G>T
|
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ENST00000537372.5:c.307G>T
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ENSP00000438296.1:p.Glu103Ter
|
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ENST00000558231.5:c.283G>T
|
ENSP00000453600.1:p.Glu95Ter
|
|
ENST00000559266.5:n.318+3086G>T
|
|
|
ENST00000559517.5:c.82G>T
|
ENSP00000453408.1:p.Glu28Ter
|
|
ENST00000561070.5:c.82G>T
|
ENSP00000452850.1:p.Glu28Ter
|
|
NM_001206897.1:c.307G>T
|
NP_001193826.1:p.Glu103Ter
|
|
NM_003888.3:c.370G>T
|
NP_003879.2:p.Glu124Ter
|
|
NM_170696.2:c.370G>T
|
NP_733797.1:p.Glu124Ter
|
|
NM_170697.2:c.82G>T
|
NP_733798.1:p.Glu28Ter
|
|
XM_024450095.1:c.370G>T
|
XP_024305863.1:p.Glu124Ter
|
|
NM_003888.4:c.370G>T
MANE Select
|
NP_003879.2:p.Glu124Ter
|
|
NM_170696.3:c.370G>T
|
NP_733797.1:p.Glu124Ter
|
|
NM_170697.3:c.82G>T
|
NP_733798.1:p.Glu28Ter
|
|
NM_001206897.2:c.307G>T
|
NP_001193826.1:p.Glu103Ter
|
|