ENST00000695651.1:n.1111C>G
|
|
|
ENST00000695652.1:c.2640C>G
|
ENSP00000512083.1:p.Ile880Met
|
|
ENST00000695653.1:c.672C>G
|
ENSP00000512084.1:p.Ile224Met
|
|
ENST00000695654.1:c.1887C>G
|
ENSP00000512085.1:p.Ile629Met
|
|
ENST00000695655.1:c.1704C>G
|
ENSP00000512086.1:n.1704C>G
|
|
ENST00000695692.1:n.2127C>G
|
|
|
ENST00000245907.11:c.2763C>G
MANE Select
|
ENSP00000245907.4:p.Ile921Met
|
|
ENST00000245907.10:c.2763C>G
|
ENSP00000245907.4:p.Ile921Met
|
|
ENST00000594005.1:n.339C>G
|
|
|
NM_000064.3:c.2763C>G
|
NP_000055.2:p.Ile921Met
|
|
NM_000064.4:c.2763C>G
MANE Select
|
NP_000055.2:p.Ile921Met
|
|