ENST00000399503.4:c.1747G>T
MANE Select
|
ENSP00000382423.3:p.Ala583Ser
|
|
ENST00000399503.3:c.1747G>T
|
ENSP00000382423.3:p.Ala583Ser
|
|
NM_005921.1:c.1747G>T
|
NP_005912.1:p.Ala583Ser
|
|
XM_005248519.3:c.1369G>T
|
XP_005248576.2:p.Ala457Ser
|
|
XM_011543406.1:c.1492G>T
|
XP_011541708.1:p.Ala498Ser
|
|
XM_011543407.1:c.1686+2087G>T
|
XP_011541709.1:n.1686+2087G>T
|
|
XM_011543408.1:c.1747G>T
|
XP_011541710.1:p.Ala583Ser
|
|
XM_017009484.1:c.1336G>T
|
XP_016864973.1:p.Ala446Ser
|
|
XM_017009485.1:c.1258G>T
|
XP_016864974.1:p.Ala420Ser
|
|
XR_001742068.2:n.1778G>T
|
|
|
NM_005921.2:c.1747G>T
MANE Select
|
NP_005912.1:p.Ala583Ser
|
|