ENST00000512123.4:c.10595T>C
MANE Select
|
ENSP00000422834.2:p.Ile3532Thr
|
|
ENST00000512123.3:c.10595T>C
|
ENSP00000422834.2:p.Ile3532Thr
|
|
NM_025074.6:c.10595T>C
|
NP_079350.5:p.Ile3532Thr
|
|
XM_006714314.1:c.10589T>C
|
XP_006714377.1:p.Ile3530Thr
|
|
XM_006714316.1:c.10367T>C
|
XP_006714379.1:p.Ile3456Thr
|
|
XM_011532270.1:c.8294T>C
|
XP_011530572.1:p.Ile2765Thr
|
|
XM_011532271.1:c.5483T>C
|
XP_011530573.1:p.Ile1828Thr
|
|
XM_006714316.3:c.10367T>C
|
XP_006714379.1:p.Ile3456Thr
|
|
NM_025074.7:c.10595T>C
MANE Select
|
NP_079350.5:p.Ile3532Thr
|
|