ENST00000245451.9:c.143G>T
MANE Select
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ENSP00000245451.4:p.Gly48Val
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ENST00000245451.8:c.143G>T
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ENSP00000245451.4:p.Gly48Val
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ENST00000417573.5:c.143G>T
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ENSP00000394165.1:p.Gly48Val
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ENST00000558961.1:c.68G>T
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ENSP00000453691.1:p.Gly23Val
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ENST00000558984.1:c.143G>T
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ENSP00000454134.1:p.Gly48Val
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ENST00000559087.5:c.143G>T
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ENSP00000453485.1:p.Gly48Val
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ENST00000559501.1:c.-47G>T
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ENSP00000453365.1:n.-47G>T
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ENST00000559642.1:c.143G>T
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ENSP00000453467.1:p.Gly48Val
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NM_001202.3:c.143G>T
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NP_001193.2:p.Gly48Val
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NM_130850.2:c.143G>T
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NP_570911.2:p.Gly48Val
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NM_130851.2:c.143G>T
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NP_570912.2:p.Gly48Val
|
|
XM_005268015.3:c.143G>T
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XP_005268072.1:p.Gly48Val
|
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NM_001202.5:c.143G>T
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NP_001193.2:p.Gly48Val
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NM_001347912.1:c.284G>T
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NP_001334841.1:p.Gly95Val
|
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NM_001347913.1:c.-47G>T
|
NP_001334842.1:n.-47G>T
|
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NM_001347914.1:c.143G>T
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NP_001334843.1:p.Gly48Val
|
|
NM_001347915.1:c.-47G>T
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NP_001334844.1:n.-47G>T
|
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NM_001347916.1:c.143G>T
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NP_001334845.1:p.Gly48Val
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NM_001347917.1:c.-47G>T
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NP_001334846.1:n.-47G>T
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NM_130850.4:c.143G>T
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NP_570911.2:p.Gly48Val
|
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NM_130851.3:c.143G>T
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NP_570912.2:p.Gly48Val
|
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NM_001202.6:c.143G>T
MANE Select
|
NP_001193.2:p.Gly48Val
|
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NM_130850.5:c.143G>T
|
NP_570911.2:p.Gly48Val
|
|
NM_001347913.2:c.-47G>T
|
NP_001334842.1:n.-47G>T
|
|
NM_001347914.2:c.143G>T
|
NP_001334843.1:p.Gly48Val
|
|
NM_001347915.2:c.-47G>T
|
NP_001334844.1:n.-47G>T
|
|
NM_130851.4:c.143G>T
|
NP_570912.2:p.Gly48Val
|
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