ENST00000695651.1:n.989C>G
|
|
|
ENST00000695652.1:c.2518C>G
|
ENSP00000512083.1:p.Arg840Gly
|
|
ENST00000695653.1:c.550C>G
|
ENSP00000512084.1:p.Arg184Gly
|
|
ENST00000695654.1:c.1765C>G
|
ENSP00000512085.1:p.Arg589Gly
|
|
ENST00000695655.1:c.1582C>G
|
ENSP00000512086.1:n.1582C>G
|
|
ENST00000695692.1:n.2005C>G
|
|
|
ENST00000245907.11:c.2641C>G
MANE Select
|
ENSP00000245907.4:p.Arg881Gly
|
|
ENST00000245907.10:c.2641C>G
|
ENSP00000245907.4:p.Arg881Gly
|
|
ENST00000594005.1:n.217C>G
|
|
|
NM_000064.3:c.2641C>G
|
NP_000055.2:p.Arg881Gly
|
|
NM_000064.4:c.2641C>G
MANE Select
|
NP_000055.2:p.Arg881Gly
|
|