ENST00000456935.7:c.1135C>G
MANE Select
|
ENSP00000395473.2:p.Pro379Ala
|
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ENST00000221363.8:c.1132C>G
|
ENSP00000221363.4:p.Pro378Ala
|
|
ENST00000456935.6:c.1135C>G
|
ENSP00000395473.2:p.Pro379Ala
|
|
ENST00000465830.1:n.299C>G
|
|
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ENST00000466794.5:n.1034C>G
|
|
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ENST00000495617.1:n.280+412C>G
|
|
|
NM_000528.3:c.1135C>G
|
NP_000519.2:p.Pro379Ala
|
|
NM_001173498.1:c.1132C>G
|
NP_001166969.1:p.Pro378Ala
|
|
XM_005259913.1:c.1138C>G
|
XP_005259970.1:p.Pro380Ala
|
|
XM_011528017.1:c.34C>G
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XP_011526319.1:p.Pro12Ala
|
|
XM_005259913.2:c.1138C>G
|
XP_005259970.1:p.Pro380Ala
|
|
XM_024451518.1:c.34C>G
|
XP_024307286.1:p.Pro12Ala
|
|
NM_000528.4:c.1135C>G
MANE Select
|
NP_000519.2:p.Pro379Ala
|
|
NM_001173498.2:c.1132C>G
|
NP_001166969.1:p.Pro378Ala
|
|