ENST00000695651.1:n.1113G>T
|
|
|
ENST00000695652.1:c.2642G>T
|
ENSP00000512083.1:p.Ser881Ile
|
|
ENST00000695653.1:c.674G>T
|
ENSP00000512084.1:p.Ser225Ile
|
|
ENST00000695654.1:c.1889G>T
|
ENSP00000512085.1:p.Ser630Ile
|
|
ENST00000695655.1:c.1706G>T
|
ENSP00000512086.1:n.1706G>T
|
|
ENST00000695692.1:n.2129G>T
|
|
|
ENST00000245907.11:c.2765G>T
MANE Select
|
ENSP00000245907.4:p.Ser922Ile
|
|
ENST00000245907.10:c.2765G>T
|
ENSP00000245907.4:p.Ser922Ile
|
|
ENST00000594005.1:n.341G>T
|
|
|
NM_000064.3:c.2765G>T
|
NP_000055.2:p.Ser922Ile
|
|
NM_000064.4:c.2765G>T
MANE Select
|
NP_000055.2:p.Ser922Ile
|
|