ENST00000369538.4:c.413G>A
|
ENSP00000358551.4:p.Arg138Gln
|
|
ENST00000520113.7:c.425G>A
MANE Select
|
ENSP00000430075.3:p.Arg142Gln
|
|
ENST00000637080.1:c.428G>A
|
ENSP00000489753.1:p.Arg143Gln
|
|
ENST00000639077.1:n.90G>A
|
|
|
ENST00000369538.3:c.512G>A
|
ENSP00000358551.3:p.Arg171Gln
|
|
ENST00000485564.3:n.299G>A
|
|
|
ENST00000520113.6:c.524G>A
|
ENSP00000430075.2:p.Arg175Gln
|
|
NM_000036.2:c.524G>A
|
NP_000027.2:p.Arg175Gln
|
|
NM_001172626.1:c.512G>A
|
NP_001166097.1:p.Arg171Gln
|
|
NM_000036.3:c.425G>A
MANE Select
|
NP_000027.3:p.Arg142Gln
|
|
NM_001172626.2:c.413G>A
|
NP_001166097.2:p.Arg138Gln
|
|