ENST00000181839.10:c.2107G>C
MANE Select
|
ENSP00000181839.4:p.Asp703His
|
|
ENST00000340829.10:c.2107G>C
|
ENSP00000340557.5:p.Asp703His
|
|
ENST00000484589.2:c.659G>C
|
|
|
ENST00000642213.1:n.589G>C
|
|
|
ENST00000643859.1:c.998G>C
|
|
|
ENST00000643915.1:c.421G>C
|
ENSP00000496187.1:p.Asp141His
|
|
ENST00000645470.1:c.37G>C
|
ENSP00000495036.1:p.Asp13His
|
|
ENST00000646039.1:c.1447G>C
|
ENSP00000494168.1:p.Asp483His
|
|
ENST00000646437.1:c.741G>C
|
|
|
ENST00000647453.1:n.1176G>C
|
|
|
ENST00000647518.1:n.3944G>C
|
|
|
ENST00000181839.8:c.2107G>C
|
ENSP00000181839.4:p.Asp703His
|
|
ENST00000340829.9:c.2107G>C
|
ENSP00000340557.5:p.Asp703His
|
|
ENST00000484589.1:n.659G>C
|
|
|
ENST00000611390.1:c.265G>C
|
ENSP00000484610.1:p.Asp89His
|
|
ENST00000613626.4:c.265G>C
|
ENSP00000480835.1:p.Asp89His
|
|
NM_003718.4:c.2107G>C
|
NP_003709.3:p.Asp703His
|
|
NM_031267.3:c.2107G>C
|
NP_112557.2:p.Asp703His
|
|
XM_011515597.1:c.2107G>C
|
XP_011513899.1:p.Asp703His
|
|
XM_011515598.1:c.2107G>C
|
XP_011513900.1:p.Asp703His
|
|
XM_011515597.3:c.2107G>C
|
XP_011513899.1:p.Asp703His
|
|
XM_017012750.2:c.2107G>C
|
XP_016868239.1:p.Asp703His
|
|
XM_017012751.2:c.2107G>C
|
XP_016868240.1:p.Asp703His
|
|
NM_003718.5:c.2107G>C
MANE Select
|
NP_003709.3:p.Asp703His
|
|