ENST00000682513.1:c.7999A>G
|
ENSP00000508201.1:p.Ile2667Val
|
|
ENST00000512123.4:c.7999A>G
MANE Select
|
ENSP00000422834.2:p.Ile2667Val
|
|
ENST00000512123.3:c.7999A>G
|
ENSP00000422834.2:p.Ile2667Val
|
|
NM_025074.6:c.7999A>G
|
NP_079350.5:p.Ile2667Val
|
|
XM_006714314.1:c.7993A>G
|
XP_006714377.1:p.Ile2665Val
|
|
XM_006714316.1:c.7771A>G
|
XP_006714379.1:p.Ile2591Val
|
|
XM_011532270.1:c.5698A>G
|
XP_011530572.1:p.Ile1900Val
|
|
XM_011532271.1:c.2887A>G
|
XP_011530573.1:p.Ile963Val
|
|
XM_006714316.3:c.7771A>G
|
XP_006714379.1:p.Ile2591Val
|
|
NM_025074.7:c.7999A>G
MANE Select
|
NP_079350.5:p.Ile2667Val
|
|