ENST00000378823.8:c.2675T>G
MANE Select
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ENSP00000368100.4:p.Val892Gly
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ENST00000638452.2:c.2378T>G
|
ENSP00000492349.2:p.Val793Gly
|
|
ENST00000638504.1:n.2283T>G
|
|
|
ENST00000638568.2:c.2378T>G
|
ENSP00000491158.2:p.Val793Gly
|
|
ENST00000639899.1:n.3194T>G
|
|
|
ENST00000640655.2:c.2378T>G
|
ENSP00000491596.2:p.Val793Gly
|
|
ENST00000651160.1:c.*819T>G
|
ENSP00000498829.1:n.*819T>G
|
|
ENST00000651723.1:c.*2758T>G
|
ENSP00000498237.1:n.*2758T>G
|
|
ENST00000652016.1:c.*892T>G
|
ENSP00000498267.1:n.*892T>G
|
|
ENST00000378823.7:c.2675T>G
|
ENSP00000368100.4:p.Val892Gly
|
|
ENST00000423956.5:c.*861T>G
|
ENSP00000390971.1:n.*861T>G
|
|
ENST00000533482.5:c.*2301T>G
|
ENSP00000431225.1:n.*2301T>G
|
|
NM_005732.3:c.2675T>G
|
NP_005723.2:p.Val892Gly
|
|
NM_005732.4:c.2675T>G
MANE Select
|
NP_005723.2:p.Val892Gly
|
|