ENST00000181839.10:c.2118T>G
MANE Select
|
ENSP00000181839.4:p.Asp706Glu
|
|
ENST00000340829.10:c.2118T>G
|
ENSP00000340557.5:p.Asp706Glu
|
|
ENST00000484589.2:c.670T>G
|
|
|
ENST00000642213.1:n.600T>G
|
|
|
ENST00000643859.1:c.1009T>G
|
|
|
ENST00000643915.1:c.432T>G
|
ENSP00000496187.1:p.Asp144Glu
|
|
ENST00000645470.1:c.48T>G
|
ENSP00000495036.1:p.Asp16Glu
|
|
ENST00000646039.1:c.1458T>G
|
ENSP00000494168.1:p.Asp486Glu
|
|
ENST00000646437.1:c.752T>G
|
|
|
ENST00000647453.1:n.1187T>G
|
|
|
ENST00000647518.1:n.3955T>G
|
|
|
ENST00000181839.8:c.2118T>G
|
ENSP00000181839.4:p.Asp706Glu
|
|
ENST00000340829.9:c.2118T>G
|
ENSP00000340557.5:p.Asp706Glu
|
|
ENST00000484589.1:n.670T>G
|
|
|
ENST00000611390.1:c.276T>G
|
ENSP00000484610.1:p.Asp92Glu
|
|
ENST00000613626.4:c.276T>G
|
ENSP00000480835.1:p.Asp92Glu
|
|
NM_003718.4:c.2118T>G
|
NP_003709.3:p.Asp706Glu
|
|
NM_031267.3:c.2118T>G
|
NP_112557.2:p.Asp706Glu
|
|
XM_011515597.1:c.2118T>G
|
XP_011513899.1:p.Asp706Glu
|
|
XM_011515598.1:c.2118T>G
|
XP_011513900.1:p.Asp706Glu
|
|
XM_011515597.3:c.2118T>G
|
XP_011513899.1:p.Asp706Glu
|
|
XM_017012750.2:c.2118T>G
|
XP_016868239.1:p.Asp706Glu
|
|
XM_017012751.2:c.2118T>G
|
XP_016868240.1:p.Asp706Glu
|
|
NM_003718.5:c.2118T>G
MANE Select
|
NP_003709.3:p.Asp706Glu
|
|