ENST00000695651.1:n.2031A>T
|
|
|
ENST00000695652.1:c.3560A>T
|
ENSP00000512083.1:p.Tyr1187Phe
|
|
ENST00000695653.1:c.1592A>T
|
ENSP00000512084.1:p.Tyr531Phe
|
|
ENST00000695654.1:c.2708A>T
|
ENSP00000512085.1:p.Tyr903Phe
|
|
ENST00000695655.1:c.2624A>T
|
ENSP00000512086.1:n.2624A>T
|
|
ENST00000695692.1:n.3047A>T
|
|
|
ENST00000245907.11:c.3683A>T
MANE Select
|
ENSP00000245907.4:p.Tyr1228Phe
|
|
ENST00000245907.10:c.3683A>T
|
ENSP00000245907.4:p.Tyr1228Phe
|
|
ENST00000596238.1:n.126A>T
|
|
|
ENST00000601008.1:c.241+495A>T
|
ENSP00000471384.1:n.241+495A>T
|
|
NM_000064.3:c.3683A>T
|
NP_000055.2:p.Tyr1228Phe
|
|
NM_000064.4:c.3683A>T
MANE Select
|
NP_000055.2:p.Tyr1228Phe
|
|