ENST00000249750.9:c.491T>G
MANE Select
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ENSP00000249750.4:p.Val164Gly
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ENST00000249750.8:c.491T>G
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ENSP00000249750.4:p.Val164Gly
|
|
ENST00000347587.7:c.491T>G
|
ENSP00000309623.3:p.Val164Gly
|
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ENST00000430119.6:c.*465T>G
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ENSP00000416754.2:n.*465T>G
|
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ENST00000537372.5:c.428T>G
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ENSP00000438296.1:p.Val143Gly
|
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ENST00000558231.5:c.404T>G
|
ENSP00000453600.1:p.Val135Gly
|
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ENST00000559266.5:n.318+3207T>G
|
|
|
ENST00000559517.5:c.203T>G
|
ENSP00000453408.1:p.Val68Gly
|
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ENST00000561070.5:c.203T>G
|
ENSP00000452850.1:p.Val68Gly
|
|
NM_001206897.1:c.428T>G
|
NP_001193826.1:p.Val143Gly
|
|
NM_003888.3:c.491T>G
|
NP_003879.2:p.Val164Gly
|
|
NM_170696.2:c.491T>G
|
NP_733797.1:p.Val164Gly
|
|
NM_170697.2:c.203T>G
|
NP_733798.1:p.Val68Gly
|
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XM_024450095.1:c.491T>G
|
XP_024305863.1:p.Val164Gly
|
|
NM_003888.4:c.491T>G
MANE Select
|
NP_003879.2:p.Val164Gly
|
|
NM_170696.3:c.491T>G
|
NP_733797.1:p.Val164Gly
|
|
NM_170697.3:c.203T>G
|
NP_733798.1:p.Val68Gly
|
|
NM_001206897.2:c.428T>G
|
NP_001193826.1:p.Val143Gly
|
|