ENST00000695651.1:n.792T>C
|
|
|
ENST00000695652.1:c.2321T>C
|
ENSP00000512083.1:p.Ile774Thr
|
|
ENST00000695653.1:c.353T>C
|
ENSP00000512084.1:p.Ile118Thr
|
|
ENST00000695654.1:c.1568T>C
|
ENSP00000512085.1:p.Ile523Thr
|
|
ENST00000695655.1:c.1385T>C
|
ENSP00000512086.1:n.1385T>C
|
|
ENST00000695692.1:n.1808T>C
|
|
|
ENST00000245907.11:c.2444T>C
MANE Select
|
ENSP00000245907.4:p.Ile815Thr
|
|
ENST00000245907.10:c.2444T>C
|
ENSP00000245907.4:p.Ile815Thr
|
|
ENST00000602053.1:n.492T>C
|
|
|
NM_000064.3:c.2444T>C
|
NP_000055.2:p.Ile815Thr
|
|
NM_000064.4:c.2444T>C
MANE Select
|
NP_000055.2:p.Ile815Thr
|
|