ENST00000369538.4:c.414G>C
|
ENSP00000358551.4:p.Arg138=
|
|
ENST00000520113.7:c.426G>C
MANE Select
|
ENSP00000430075.3:p.Arg142=
|
|
ENST00000637080.1:c.429G>C
|
ENSP00000489753.1:p.Arg143=
|
|
ENST00000639077.1:n.91G>C
|
|
|
ENST00000369538.3:c.513G>C
|
ENSP00000358551.3:p.Arg171=
|
|
ENST00000485564.3:n.300G>C
|
|
|
ENST00000520113.6:c.525G>C
|
ENSP00000430075.2:p.Arg175=
|
|
NM_000036.2:c.525G>C
|
NP_000027.2:p.Arg175=
|
|
NM_001172626.1:c.513G>C
|
NP_001166097.1:p.Arg171=
|
|
NM_000036.3:c.426G>C
MANE Select
|
NP_000027.3:p.Arg142=
|
|
NM_001172626.2:c.414G>C
|
NP_001166097.2:p.Arg138=
|
|