ENST00000367408.6:n.2440G>T
|
|
|
ENST00000367409.9:c.9153G>T
MANE Select
|
ENSP00000356379.4:p.Arg3051=
|
|
ENST00000680265.1:c.9375G>T
|
ENSP00000505384.1:p.Arg3125=
|
|
ENST00000680710.1:c.9153G>T
|
ENSP00000506676.1:p.Arg3051=
|
|
ENST00000294732.11:c.4398G>T
|
ENSP00000294732.7:p.Arg1466=
|
|
ENST00000367408.5:c.2148G>T
|
ENSP00000356378.1:p.Arg716=
|
|
ENST00000367409.8:c.9153G>T
|
ENSP00000356379.4:p.Arg3051=
|
|
ENST00000612785.1:c.3111G>T
|
ENSP00000479244.1:p.Arg1037=
|
|
NM_001206846.1:c.4398G>T
|
NP_001193775.1:p.Arg1466=
|
|
NM_018136.4:c.9153G>T
|
NP_060606.3:p.Arg3051=
|
|
NM_018136.5:c.9153G>T
MANE Select
|
NP_060606.3:p.Arg3051=
|
|
NM_001206846.2:c.4398G>T
|
NP_001193775.1:p.Arg1466=
|
|