ENST00000512123.4:c.10129G>A
MANE Select
|
ENSP00000422834.2:p.Val3377Ile
|
|
ENST00000512123.3:c.10129G>A
|
ENSP00000422834.2:p.Val3377Ile
|
|
NM_025074.6:c.10129G>A
|
NP_079350.5:p.Val3377Ile
|
|
XM_006714314.1:c.10123G>A
|
XP_006714377.1:p.Val3375Ile
|
|
XM_006714316.1:c.9901G>A
|
XP_006714379.1:p.Val3301Ile
|
|
XM_011532270.1:c.7828G>A
|
XP_011530572.1:p.Val2610Ile
|
|
XM_011532271.1:c.5017G>A
|
XP_011530573.1:p.Val1673Ile
|
|
XM_006714316.3:c.9901G>A
|
XP_006714379.1:p.Val3301Ile
|
|
NM_025074.7:c.10129G>A
MANE Select
|
NP_079350.5:p.Val3377Ile
|
|