ENST00000181839.10:c.2134G>C
MANE Select
|
ENSP00000181839.4:p.Gly712Arg
|
|
ENST00000340829.10:c.2134G>C
|
ENSP00000340557.5:p.Gly712Arg
|
|
ENST00000484589.2:c.686G>C
|
|
|
ENST00000642213.1:n.616G>C
|
|
|
ENST00000643859.1:c.1025G>C
|
|
|
ENST00000643915.1:c.448G>C
|
ENSP00000496187.1:p.Gly150Arg
|
|
ENST00000645470.1:c.64G>C
|
ENSP00000495036.1:p.Gly22Arg
|
|
ENST00000646039.1:c.1474G>C
|
ENSP00000494168.1:p.Gly492Arg
|
|
ENST00000646437.1:c.768G>C
|
|
|
ENST00000647453.1:n.1203G>C
|
|
|
ENST00000647518.1:n.3971G>C
|
|
|
ENST00000181839.8:c.2134G>C
|
ENSP00000181839.4:p.Gly712Arg
|
|
ENST00000340829.9:c.2134G>C
|
ENSP00000340557.5:p.Gly712Arg
|
|
ENST00000484589.1:n.686G>C
|
|
|
ENST00000611390.1:c.292G>C
|
ENSP00000484610.1:p.Gly98Arg
|
|
ENST00000613626.4:c.292G>C
|
ENSP00000480835.1:p.Gly98Arg
|
|
NM_003718.4:c.2134G>C
|
NP_003709.3:p.Gly712Arg
|
|
NM_031267.3:c.2134G>C
|
NP_112557.2:p.Gly712Arg
|
|
XM_011515597.1:c.2134G>C
|
XP_011513899.1:p.Gly712Arg
|
|
XM_011515598.1:c.2134G>C
|
XP_011513900.1:p.Gly712Arg
|
|
XM_011515597.3:c.2134G>C
|
XP_011513899.1:p.Gly712Arg
|
|
XM_017012750.2:c.2134G>C
|
XP_016868239.1:p.Gly712Arg
|
|
XM_017012751.2:c.2134G>C
|
XP_016868240.1:p.Gly712Arg
|
|
NM_003718.5:c.2134G>C
MANE Select
|
NP_003709.3:p.Gly712Arg
|
|