|
NM_002601.4:c.182G>A
MANE Select
|
NP_002592.1:p.Arg61Gln
|
|
ENST00000287600.9:c.182G>A
MANE Select
|
ENSP00000287600.4:p.Arg61Gln
|
|
NM_001291018.1:c.182G>A
|
NP_001277947.1:p.Arg61Gln
|
|
NM_001291018.2:c.182G>A
|
NP_001277947.1:p.Arg61Gln
|
|
NM_002601.3:c.182G>A
|
NP_002592.1:p.Arg61Gln
|
|
ENST00000287600.8:c.182G>A
|
ENSP00000287600.4:p.Arg61Gln
|
|
ENST00000409772.5:c.182G>A
|
ENSP00000387108.1:p.Arg61Gln
|
|
ENST00000428104.2:c.125G>A
|
ENSP00000399098.2:p.Arg42Gln
|
|
ENST00000486044.1:n.331G>A
|
|
|
XM_011511342.1:c.125G>A
|
XP_011509644.1:p.Arg42Gln
|