ENST00000695651.1:n.1011T>C
|
|
|
ENST00000695652.1:c.2540T>C
|
ENSP00000512083.1:p.Ile847Thr
|
|
ENST00000695653.1:c.572T>C
|
ENSP00000512084.1:p.Ile191Thr
|
|
ENST00000695654.1:c.1787T>C
|
ENSP00000512085.1:p.Ile596Thr
|
|
ENST00000695655.1:c.1604T>C
|
ENSP00000512086.1:n.1604T>C
|
|
ENST00000695692.1:n.2027T>C
|
|
|
ENST00000245907.11:c.2663T>C
MANE Select
|
ENSP00000245907.4:p.Ile888Thr
|
|
ENST00000245907.10:c.2663T>C
|
ENSP00000245907.4:p.Ile888Thr
|
|
ENST00000594005.1:n.239T>C
|
|
|
NM_000064.3:c.2663T>C
|
NP_000055.2:p.Ile888Thr
|
|
NM_000064.4:c.2663T>C
MANE Select
|
NP_000055.2:p.Ile888Thr
|
|