ENST00000682422.1:n.800T>G
|
|
|
ENST00000682545.1:c.*225T>G
|
ENSP00000508402.1:n.*225T>G
|
|
ENST00000682887.1:c.1620T>G
|
ENSP00000506946.1:n.1620T>G
|
|
ENST00000683302.1:c.1150T>G
|
ENSP00000507885.1:p.Phe384Val
|
|
ENST00000683557.1:c.*51T>G
|
ENSP00000508029.1:n.*51T>G
|
|
ENST00000367282.6:c.1219T>G
MANE Select
|
ENSP00000356251.4:p.Phe407Val
|
|
ENST00000367282.5:c.1219T>G
|
ENSP00000356251.4:p.Phe407Val
|
|
NM_004767.3:c.1219T>G
|
NP_004758.3:p.Phe407Val
|
|
XM_011510158.1:c.658T>G
|
XP_011508460.1:p.Phe220Val
|
|
NM_004767.4:c.1219T>G
|
NP_004758.3:p.Phe407Val
|
|
XM_011510158.2:c.658T>G
|
XP_011508460.1:p.Phe220Val
|
|
NM_004767.5:c.1219T>G
MANE Select
|
NP_004758.3:p.Phe407Val
|
|