ENST00000399503.4:c.2618T>G
MANE Select
|
ENSP00000382423.3:p.Val873Gly
|
|
ENST00000399503.3:c.2618T>G
|
ENSP00000382423.3:p.Val873Gly
|
|
NM_005921.1:c.2618T>G
|
NP_005912.1:p.Val873Gly
|
|
XM_005248519.3:c.2240T>G
|
XP_005248576.2:p.Val747Gly
|
|
XM_011543406.1:c.2363T>G
|
XP_011541708.1:p.Val788Gly
|
|
XM_011543407.1:c.2339T>G
|
XP_011541709.1:p.Val780Gly
|
|
XM_011543408.1:c.2618T>G
|
XP_011541710.1:p.Val873Gly
|
|
XM_017009484.1:c.2207T>G
|
XP_016864973.1:p.Val736Gly
|
|
XM_017009485.1:c.2129T>G
|
XP_016864974.1:p.Val710Gly
|
|
XR_001742068.2:n.2649T>G
|
|
|
NM_005921.2:c.2618T>G
MANE Select
|
NP_005912.1:p.Val873Gly
|
|