ENST00000399503.4:c.2619A>G
MANE Select
|
ENSP00000382423.3:p.Val873=
|
|
ENST00000399503.3:c.2619A>G
|
ENSP00000382423.3:p.Val873=
|
|
NM_005921.1:c.2619A>G
|
NP_005912.1:p.Val873=
|
|
XM_005248519.3:c.2241A>G
|
XP_005248576.2:p.Val747=
|
|
XM_011543406.1:c.2364A>G
|
XP_011541708.1:p.Val788=
|
|
XM_011543407.1:c.2340A>G
|
XP_011541709.1:p.Val780=
|
|
XM_011543408.1:c.2619A>G
|
XP_011541710.1:p.Val873=
|
|
XM_017009484.1:c.2208A>G
|
XP_016864973.1:p.Val736=
|
|
XM_017009485.1:c.2130A>G
|
XP_016864974.1:p.Val710=
|
|
XR_001742068.2:n.2650A>G
|
|
|
NM_005921.2:c.2619A>G
MANE Select
|
NP_005912.1:p.Val873=
|
|