ENST00000695651.1:n.806C>G
|
|
|
ENST00000695652.1:c.2335C>G
|
ENSP00000512083.1:p.Pro779Ala
|
|
ENST00000695653.1:c.367C>G
|
ENSP00000512084.1:p.Pro123Ala
|
|
ENST00000695654.1:c.1582C>G
|
ENSP00000512085.1:p.Pro528Ala
|
|
ENST00000695655.1:c.1399C>G
|
ENSP00000512086.1:n.1399C>G
|
|
ENST00000695692.1:n.1822C>G
|
|
|
ENST00000245907.11:c.2458C>G
MANE Select
|
ENSP00000245907.4:p.Pro820Ala
|
|
ENST00000245907.10:c.2458C>G
|
ENSP00000245907.4:p.Pro820Ala
|
|
ENST00000602053.1:n.506C>G
|
|
|
NM_000064.3:c.2458C>G
|
NP_000055.2:p.Pro820Ala
|
|
NM_000064.4:c.2458C>G
MANE Select
|
NP_000055.2:p.Pro820Ala
|
|