ENST00000369538.4:c.458G>C
|
ENSP00000358551.4:p.Arg153Thr
|
|
ENST00000520113.7:c.470G>C
MANE Select
|
ENSP00000430075.3:p.Arg157Thr
|
|
ENST00000637080.1:c.473G>C
|
ENSP00000489753.1:p.Arg158Thr
|
|
ENST00000639077.1:n.135G>C
|
|
|
ENST00000369538.3:c.557G>C
|
ENSP00000358551.3:p.Arg186Thr
|
|
ENST00000485564.3:n.344G>C
|
|
|
ENST00000520113.6:c.569G>C
|
ENSP00000430075.2:p.Arg190Thr
|
|
NM_000036.2:c.569G>C
|
NP_000027.2:p.Arg190Thr
|
|
NM_001172626.1:c.557G>C
|
NP_001166097.1:p.Arg186Thr
|
|
NM_000036.3:c.470G>C
MANE Select
|
NP_000027.3:p.Arg157Thr
|
|
NM_001172626.2:c.458G>C
|
NP_001166097.2:p.Arg153Thr
|
|