ENST00000399503.4:c.2618T>A
MANE Select
|
ENSP00000382423.3:p.Val873Glu
|
|
ENST00000399503.3:c.2618T>A
|
ENSP00000382423.3:p.Val873Glu
|
|
NM_005921.1:c.2618T>A
|
NP_005912.1:p.Val873Glu
|
|
XM_005248519.3:c.2240T>A
|
XP_005248576.2:p.Val747Glu
|
|
XM_011543406.1:c.2363T>A
|
XP_011541708.1:p.Val788Glu
|
|
XM_011543407.1:c.2339T>A
|
XP_011541709.1:p.Val780Glu
|
|
XM_011543408.1:c.2618T>A
|
XP_011541710.1:p.Val873Glu
|
|
XM_017009484.1:c.2207T>A
|
XP_016864973.1:p.Val736Glu
|
|
XM_017009485.1:c.2129T>A
|
XP_016864974.1:p.Val710Glu
|
|
XR_001742068.2:n.2649T>A
|
|
|
NM_005921.2:c.2618T>A
MANE Select
|
NP_005912.1:p.Val873Glu
|
|