ENST00000480266.6:c.414C>G
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ENSP00000479015.1:p.Ala138=
|
|
ENST00000373203.9:c.960C>G
MANE Select
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ENSP00000362299.4:p.Ala320=
|
|
ENST00000344849.4:c.960C>G
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ENSP00000341917.3:p.Ala320=
|
|
ENST00000373203.8:c.960C>G
|
ENSP00000362299.4:p.Ala320=
|
|
ENST00000480266.5:c.414C>G
|
ENSP00000479015.1:p.Ala138=
|
|
NM_000118.3:c.960C>G , LRG_589t1:c.960C>G
|
NP_000109.1:p.Ala320=
|
|
NM_001114753.2:c.960C>G , LRG_589t2:c.960C>G
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NP_001108225.1:p.Ala320=
|
|
NM_001278138.1:c.414C>G
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NP_001265067.1:p.Ala138=
|
|
NM_001114753.3:c.960C>G
MANE Select
|
NP_001108225.1:p.Ala320=
|
|
NM_001278138.2:c.414C>G
|
NP_001265067.1:p.Ala138=
|
|