|
NM_025074.7:c.10999C>T
MANE Select
|
NP_079350.5:p.Gln3667Ter
|
|
ENST00000512123.4:c.10999C>T
MANE Select
|
ENSP00000422834.2:p.Gln3667Ter
|
|
NM_025074.6:c.10999C>T
|
NP_079350.5:p.Gln3667Ter
|
|
ENST00000512123.3:c.10999C>T
|
ENSP00000422834.2:p.Gln3667Ter
|
|
XM_006714314.1:c.10993C>T
|
XP_006714377.1:p.Gln3665Ter
|
|
XM_006714316.1:c.10771C>T
|
XP_006714379.1:p.Gln3591Ter
|
|
XM_006714316.3:c.10771C>T
|
XP_006714379.1:p.Gln3591Ter
|
|
XM_011532270.1:c.8698C>T
|
XP_011530572.1:p.Gln2900Ter
|
|
XM_011532271.1:c.5887C>T
|
XP_011530573.1:p.Gln1963Ter
|