ENST00000695651.1:n.863G>T
|
|
|
ENST00000695652.1:c.2392G>T
|
ENSP00000512083.1:p.Val798Phe
|
|
ENST00000695653.1:c.424G>T
|
ENSP00000512084.1:p.Val142Phe
|
|
ENST00000695654.1:c.1639G>T
|
ENSP00000512085.1:p.Val547Phe
|
|
ENST00000695655.1:c.1456G>T
|
ENSP00000512086.1:n.1456G>T
|
|
ENST00000695692.1:n.1879G>T
|
|
|
ENST00000245907.11:c.2515G>T
MANE Select
|
ENSP00000245907.4:p.Val839Phe
|
|
ENST00000245907.10:c.2515G>T
|
ENSP00000245907.4:p.Val839Phe
|
|
ENST00000602053.1:n.563G>T
|
|
|
NM_000064.3:c.2515G>T
|
NP_000055.2:p.Val839Phe
|
|
NM_000064.4:c.2515G>T
MANE Select
|
NP_000055.2:p.Val839Phe
|
|