ENST00000399503.4:c.2618T>C
MANE Select
|
ENSP00000382423.3:p.Val873Ala
|
|
ENST00000399503.3:c.2618T>C
|
ENSP00000382423.3:p.Val873Ala
|
|
NM_005921.1:c.2618T>C
|
NP_005912.1:p.Val873Ala
|
|
XM_005248519.3:c.2240T>C
|
XP_005248576.2:p.Val747Ala
|
|
XM_011543406.1:c.2363T>C
|
XP_011541708.1:p.Val788Ala
|
|
XM_011543407.1:c.2339T>C
|
XP_011541709.1:p.Val780Ala
|
|
XM_011543408.1:c.2618T>C
|
XP_011541710.1:p.Val873Ala
|
|
XM_017009484.1:c.2207T>C
|
XP_016864973.1:p.Val736Ala
|
|
XM_017009485.1:c.2129T>C
|
XP_016864974.1:p.Val710Ala
|
|
XR_001742068.2:n.2649T>C
|
|
|
NM_005921.2:c.2618T>C
MANE Select
|
NP_005912.1:p.Val873Ala
|
|