ENST00000382103.7:c.370G>T
MANE Select
|
ENSP00000371535.2:p.Asp124Tyr
|
|
ENST00000680581.1:c.370G>T
|
ENSP00000506483.1:p.Asp124Tyr
|
|
ENST00000680824.1:n.1586G>T
|
|
|
ENST00000681071.1:n.662G>T
|
|
|
ENST00000681166.1:n.1417G>T
|
|
|
ENST00000681341.1:n.1511G>T
|
|
|
ENST00000681640.1:n.464G>T
|
|
|
ENST00000681948.1:c.625G>T
|
ENSP00000505991.1:p.Asp209Tyr
|
|
ENST00000358971.7:c.*168G>T
|
ENSP00000351857.3:n.*168G>T
|
|
ENST00000382103.6:c.370G>T
|
ENSP00000371535.2:p.Asp124Tyr
|
|
ENST00000514585.5:c.*71G>T
|
ENSP00000421880.1:n.*71G>T
|
|
NM_016955.3:c.370G>T
|
NP_058651.3:p.Asp124Tyr
|
|
XM_005248168.2:c.133G>T
|
XP_005248225.1:p.Asp45Tyr
|
|
XM_006713965.2:c.190G>T
|
XP_006714028.1:p.Asp64Tyr
|
|
XM_011513846.1:c.367G>T
|
XP_011512148.1:p.Asp123Tyr
|
|
XM_011513847.1:c.337G>T
|
XP_011512149.1:p.Asp113Tyr
|
|
XM_011513848.1:c.190G>T
|
XP_011512150.1:p.Asp64Tyr
|
|
XM_011513846.2:c.367G>T
|
XP_011512148.1:p.Asp123Tyr
|
|
XM_011513847.2:c.337G>T
|
XP_011512149.1:p.Asp113Tyr
|
|
XM_017008277.1:c.625G>T
|
XP_016863766.1:p.Asp209Tyr
|
|
XM_017008278.1:c.-54G>T
|
XP_016863767.1:n.-54G>T
|
|
NM_016955.4:c.370G>T
MANE Select
|
NP_058651.3:p.Asp124Tyr
|
|