ENST00000356839.10:c.1037C>T
MANE Select
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ENSP00000349297.5:p.Ala346Val
|
|
ENST00000322910.9:c.*992C>T
|
ENSP00000325395.5:n.*992C>T
|
|
ENST00000350303.9:c.971C>T
|
ENSP00000344152.5:p.Ala324Val
|
|
ENST00000356839.9:c.1037C>T
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ENSP00000349297.5:p.Ala346Val
|
|
ENST00000543245.6:c.1106C>T
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ENSP00000438689.2:p.Ala369Val
|
|
ENST00000578824.5:n.186C>T
|
|
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ENST00000582379.1:n.421C>T
|
|
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ENST00000583858.5:c.66C>T
|
|
|
NM_000018.3:c.1037C>T
|
NP_000009.1:p.Ala346Val
|
|
NM_001033859.2:c.971C>T
|
NP_001029031.1:p.Ala324Val
|
|
NM_001270447.1:c.1106C>T
|
NP_001257376.1:p.Ala369Val
|
|
NM_001270448.1:c.809C>T
|
NP_001257377.1:p.Ala270Val
|
|
XM_006721516.2:c.1037C>T
|
XP_006721579.2:p.Ala346Val
|
|
XM_011523829.1:c.1037C>T
|
XP_011522131.1:p.Ala346Val
|
|
XM_011523830.1:c.1037C>T
|
XP_011522132.1:p.Ala346Val
|
|
XR_934021.1:n.1144C>T
|
|
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XR_934022.1:n.1144C>T
|
|
|
XR_934023.1:n.1144C>T
|
|
|
XM_006721516.3:c.1037C>T
|
XP_006721579.2:p.Ala346Val
|
|
XM_011523829.2:c.1037C>T
|
XP_011522131.1:p.Ala346Val
|
|
XM_011523830.2:c.1037C>T
|
XP_011522132.1:p.Ala346Val
|
|
XM_024450741.1:c.1037C>T
|
XP_024306509.1:p.Ala346Val
|
|
XR_934021.2:n.1096C>T
|
|
|
XR_934022.2:n.1096C>T
|
|
|
XR_934023.2:n.1096C>T
|
|
|
NM_000018.4:c.1037C>T
MANE Select
|
NP_000009.1:p.Ala346Val
|
|
NM_001033859.3:c.971C>T
|
NP_001029031.1:p.Ala324Val
|
|
NM_001270447.2:c.1106C>T
|
NP_001257376.1:p.Ala369Val
|
|
NM_001270448.2:c.809C>T
|
NP_001257377.1:p.Ala270Val
|
|