ENST00000695651.1:n.2097C>G
|
|
|
ENST00000695652.1:c.3626C>G
|
ENSP00000512083.1:p.Pro1209Arg
|
|
ENST00000695653.1:c.1658C>G
|
ENSP00000512084.1:p.Pro553Arg
|
|
ENST00000695654.1:c.2774C>G
|
ENSP00000512085.1:p.Pro925Arg
|
|
ENST00000695655.1:c.2690C>G
|
ENSP00000512086.1:n.2690C>G
|
|
ENST00000695692.1:n.3113C>G
|
|
|
ENST00000245907.11:c.3749C>G
MANE Select
|
ENSP00000245907.4:p.Pro1250Arg
|
|
ENST00000245907.10:c.3749C>G
|
ENSP00000245907.4:p.Pro1250Arg
|
|
ENST00000596238.1:n.192C>G
|
|
|
ENST00000601008.1:c.241+561C>G
|
ENSP00000471384.1:n.241+561C>G
|
|
NM_000064.3:c.3749C>G
|
NP_000055.2:p.Pro1250Arg
|
|
NM_000064.4:c.3749C>G
MANE Select
|
NP_000055.2:p.Pro1250Arg
|
|