ENST00000456935.7:c.1052T>G
MANE Select
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ENSP00000395473.2:p.Val351Gly
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ENST00000221363.8:c.1049T>G
|
ENSP00000221363.4:p.Val350Gly
|
|
ENST00000456935.6:c.1052T>G
|
ENSP00000395473.2:p.Val351Gly
|
|
ENST00000465830.1:n.133T>G
|
|
|
ENST00000466794.5:n.1009-141T>G
|
|
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ENST00000495617.1:n.280+246T>G
|
|
|
NM_000528.3:c.1052T>G
|
NP_000519.2:p.Val351Gly
|
|
NM_001173498.1:c.1049T>G
|
NP_001166969.1:p.Val350Gly
|
|
XM_005259913.1:c.1055T>G
|
XP_005259970.1:p.Val352Gly
|
|
XM_011528017.1:c.9-141T>G
|
XP_011526319.1:n.9-141T>G
|
|
XM_005259913.2:c.1055T>G
|
XP_005259970.1:p.Val352Gly
|
|
XM_024451518.1:c.9-141T>G
|
XP_024307286.1:n.9-141T>G
|
|
NM_000528.4:c.1052T>G
MANE Select
|
NP_000519.2:p.Val351Gly
|
|
NM_001173498.2:c.1049T>G
|
NP_001166969.1:p.Val350Gly
|
|