ENST00000409155.8:c.254T>C
MANE Select
|
ENSP00000386284.3:p.Val85Ala
|
|
ENST00000409155.7:c.254T>C
|
ENSP00000386284.3:p.Val85Ala
|
|
ENST00000448137.5:c.281T>C
|
ENSP00000392748.1:p.Val94Ala
|
|
ENST00000464749.5:n.258-601T>C
|
|
|
ENST00000468504.5:n.376T>C
|
|
|
ENST00000482001.1:n.527T>C
|
|
|
ENST00000482847.5:n.527T>C
|
|
|
NM_000031.5:c.254T>C
|
NP_000022.3:p.Val85Ala
|
|
XM_005251799.1:c.341T>C
|
XP_005251856.1:p.Val114Ala
|
|
XM_011518363.1:c.380T>C
|
XP_011516665.1:p.Val127Ala
|
|
XM_011518364.1:c.281T>C
|
XP_011516666.1:p.Val94Ala
|
|
NM_001003945.2:c.341T>C
|
NP_001003945.1:p.Val114Ala
|
|
NM_001317745.1:c.230T>C
|
NP_001304674.1:p.Val77Ala
|
|
XM_011518364.2:c.281T>C
|
XP_011516666.1:p.Val94Ala
|
|
XM_024447449.1:c.341T>C
|
XP_024303217.1:p.Val114Ala
|
|
XR_002956764.1:n.754T>C
|
|
|
NM_000031.6:c.254T>C
MANE Select
|
NP_000022.3:p.Val85Ala
|
|
NM_001003945.3:c.341T>C
|
NP_001003945.1:p.Val114Ala
|
|
NM_001317745.2:c.230T>C
|
NP_001304674.1:p.Val77Ala
|
|