ENST00000399503.4:c.2013G>A
MANE Select
|
ENSP00000382423.3:p.Ala671=
|
|
ENST00000399503.3:c.2013G>A
|
ENSP00000382423.3:p.Ala671=
|
|
NM_005921.1:c.2013G>A
|
NP_005912.1:p.Ala671=
|
|
XM_005248519.3:c.1635G>A
|
XP_005248576.2:p.Ala545=
|
|
XM_011543406.1:c.1758G>A
|
XP_011541708.1:p.Ala586=
|
|
XM_011543407.1:c.1734G>A
|
XP_011541709.1:p.Ala578=
|
|
XM_011543408.1:c.2013G>A
|
XP_011541710.1:p.Ala671=
|
|
XM_017009484.1:c.1602G>A
|
XP_016864973.1:p.Ala534=
|
|
XM_017009485.1:c.1524G>A
|
XP_016864974.1:p.Ala508=
|
|
XR_001742068.2:n.2044G>A
|
|
|
NM_005921.2:c.2013G>A
MANE Select
|
NP_005912.1:p.Ala671=
|
|