ENST00000675795.1:c.985C>G
MANE Select
|
ENSP00000501699.1:p.Pro329Ala
|
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ENST00000286301.7:c.985C>G
|
ENSP00000286301.3:p.Pro329Ala
|
|
ENST00000504875.5:c.985C>G
|
ENSP00000422212.1:p.Pro329Ala
|
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ENST00000543093.1:c.890-2827C>G
|
ENSP00000445282.1:n.890-2827C>G
|
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NM_001288705.1:c.985C>G
|
NP_001275634.1:p.Pro329Ala
|
|
NM_005211.3:c.985C>G
|
NP_005202.2:p.Pro329Ala
|
|
NR_109969.1:n.1198C>G
|
|
|
NM_001288705.2:c.985C>G
|
NP_001275634.1:p.Pro329Ala
|
|
NM_001349736.1:c.985C>G
|
NP_001336665.1:p.Pro329Ala
|
|
NM_001288705.3:c.985C>G
MANE Select
|
NP_001275634.1:p.Pro329Ala
|
|
NM_001375320.1:c.985C>G
|
NP_001362249.1:p.Pro329Ala
|
|
NM_001375321.1:c.541C>G
|
NP_001362250.1:p.Pro181Ala
|
|
NR_164679.1:n.1041C>G
|
|
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NM_001349736.2:c.985C>G
|
NP_001336665.1:p.Pro329Ala
|
|
NM_005211.4:c.985C>G
|
NP_005202.2:p.Pro329Ala
|
|
NR_109969.2:n.1112C>G
|
|
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