ENST00000695651.1:n.1047T>C
|
|
|
ENST00000695652.1:c.2576T>C
|
ENSP00000512083.1:p.Ile859Thr
|
|
ENST00000695653.1:c.608T>C
|
ENSP00000512084.1:p.Ile203Thr
|
|
ENST00000695654.1:c.1823T>C
|
ENSP00000512085.1:p.Ile608Thr
|
|
ENST00000695655.1:c.1640T>C
|
ENSP00000512086.1:n.1640T>C
|
|
ENST00000695692.1:n.2063T>C
|
|
|
ENST00000245907.11:c.2699T>C
MANE Select
|
ENSP00000245907.4:p.Ile900Thr
|
|
ENST00000245907.10:c.2699T>C
|
ENSP00000245907.4:p.Ile900Thr
|
|
ENST00000594005.1:n.275T>C
|
|
|
NM_000064.3:c.2699T>C
|
NP_000055.2:p.Ile900Thr
|
|
NM_000064.4:c.2699T>C
MANE Select
|
NP_000055.2:p.Ile900Thr
|
|