ENST00000409155.8:c.896C>T
MANE Select
|
ENSP00000386284.3:p.Ala299Val
|
|
ENST00000409155.7:c.896C>T
|
ENSP00000386284.3:p.Ala299Val
|
|
ENST00000482847.5:n.1169C>T
|
|
|
NM_000031.5:c.896C>T
|
NP_000022.3:p.Ala299Val
|
|
XM_005251799.1:c.983C>T
|
XP_005251856.1:p.Ala328Val
|
|
XM_011518363.1:c.1022C>T
|
XP_011516665.1:p.Ala341Val
|
|
XM_011518364.1:c.923C>T
|
XP_011516666.1:p.Ala308Val
|
|
NM_001003945.2:c.983C>T
|
NP_001003945.1:p.Ala328Val
|
|
NM_001317745.1:c.872C>T
|
NP_001304674.1:p.Ala291Val
|
|
XM_011518364.2:c.923C>T
|
XP_011516666.1:p.Ala308Val
|
|
XM_024447449.1:c.983C>T
|
XP_024303217.1:p.Ala328Val
|
|
NM_000031.6:c.896C>T
MANE Select
|
NP_000022.3:p.Ala299Val
|
|
NM_001003945.3:c.983C>T
|
NP_001003945.1:p.Ala328Val
|
|
NM_001317745.2:c.872C>T
|
NP_001304674.1:p.Ala291Val
|
|