ENST00000378823.8:c.3335G=
MANE Select
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ENSP00000368100.4:p.Arg1112=
|
|
ENST00000638452.2:c.3038G=
|
ENSP00000492349.2:p.Arg1013=
|
|
ENST00000638504.1:n.2943G=
|
|
|
ENST00000638568.2:c.3038G=
|
ENSP00000491158.2:p.Arg1013=
|
|
ENST00000639899.1:n.3854G=
|
|
|
ENST00000640655.2:c.3038G=
|
ENSP00000491596.2:p.Arg1013=
|
|
ENST00000651249.1:c.171G=
|
|
|
ENST00000378823.7:c.3335G=
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ENSP00000368100.4:p.Arg1112=
|
|
ENST00000533482.5:c.*2961G=
|
ENSP00000431225.1:n.*2961G=
|
|
NM_005732.3:c.3335G=
|
NP_005723.2:p.Arg1112=
|
|
NM_005732.4:c.3335G=
MANE Select
|
NP_005723.2:p.Arg1112=
|
|