ENST00000369538.4:c.459G=
|
ENSP00000358551.4:p.Arg153=
|
|
ENST00000520113.7:c.471G=
MANE Select
|
ENSP00000430075.3:p.Arg157=
|
|
ENST00000637080.1:c.474G=
|
ENSP00000489753.1:p.Arg158=
|
|
ENST00000639077.1:n.136G=
|
|
|
ENST00000369538.3:c.558G=
|
ENSP00000358551.3:p.Arg186=
|
|
ENST00000485564.3:n.345G=
|
|
|
ENST00000520113.6:c.570G=
|
ENSP00000430075.2:p.Arg190=
|
|
NM_000036.2:c.570G=
|
NP_000027.2:p.Arg190=
|
|
NM_001172626.1:c.558G=
|
NP_001166097.1:p.Arg186=
|
|
NM_000036.3:c.471G=
MANE Select
|
NP_000027.3:p.Arg157=
|
|
NM_001172626.2:c.459G=
|
NP_001166097.2:p.Arg153=
|
|