ENST00000695651.1:n.1016C>T
|
|
|
ENST00000695652.1:c.2545C>T
|
ENSP00000512083.1:p.Pro849Ser
|
|
ENST00000695653.1:c.577C>T
|
ENSP00000512084.1:p.Pro193Ser
|
|
ENST00000695654.1:c.1792C>T
|
ENSP00000512085.1:p.Pro598Ser
|
|
ENST00000695655.1:c.1609C>T
|
ENSP00000512086.1:n.1609C>T
|
|
ENST00000695692.1:n.2032C>T
|
|
|
ENST00000245907.11:c.2668C>T
MANE Select
|
ENSP00000245907.4:p.Pro890Ser
|
|
ENST00000245907.10:c.2668C>T
|
ENSP00000245907.4:p.Pro890Ser
|
|
ENST00000594005.1:n.244C>T
|
|
|
NM_000064.3:c.2668C>T
|
NP_000055.2:p.Pro890Ser
|
|
NM_000064.4:c.2668C>T
MANE Select
|
NP_000055.2:p.Pro890Ser
|
|