ENST00000382103.7:c.385G>T
MANE Select
|
ENSP00000371535.2:p.Ala129Ser
|
|
ENST00000680581.1:c.385G>T
|
ENSP00000506483.1:p.Ala129Ser
|
|
ENST00000680824.1:n.1601G>T
|
|
|
ENST00000681071.1:n.677G>T
|
|
|
ENST00000681166.1:n.1432G>T
|
|
|
ENST00000681341.1:n.1526G>T
|
|
|
ENST00000681640.1:n.479G>T
|
|
|
ENST00000681948.1:c.640G>T
|
ENSP00000505991.1:p.Ala214Ser
|
|
ENST00000358971.7:c.*183G>T
|
ENSP00000351857.3:n.*183G>T
|
|
ENST00000382103.6:c.385G>T
|
ENSP00000371535.2:p.Ala129Ser
|
|
ENST00000514585.5:c.*86G>T
|
ENSP00000421880.1:n.*86G>T
|
|
NM_016955.3:c.385G>T
|
NP_058651.3:p.Ala129Ser
|
|
XM_005248168.2:c.148G>T
|
XP_005248225.1:p.Ala50Ser
|
|
XM_006713965.2:c.205G>T
|
XP_006714028.1:p.Ala69Ser
|
|
XM_011513846.1:c.382G>T
|
XP_011512148.1:p.Ala128Ser
|
|
XM_011513847.1:c.352G>T
|
XP_011512149.1:p.Ala118Ser
|
|
XM_011513848.1:c.205G>T
|
XP_011512150.1:p.Ala69Ser
|
|
XM_011513846.2:c.382G>T
|
XP_011512148.1:p.Ala128Ser
|
|
XM_011513847.2:c.352G>T
|
XP_011512149.1:p.Ala118Ser
|
|
XM_017008277.1:c.640G>T
|
XP_016863766.1:p.Ala214Ser
|
|
XM_017008278.1:c.-39G>T
|
XP_016863767.1:n.-39G>T
|
|
NM_016955.4:c.385G>T
MANE Select
|
NP_058651.3:p.Ala129Ser
|
|