|
NM_013432.5:c.2623C>T
(TONSL)
MANE Select
|
NP_038460.4:p.Arg875Ter
|
|
ENST00000409379.8:c.2623C>T
(TONSL)
MANE Select
|
ENSP00000386239.3:p.Arg875Ter
|
|
NM_013432.4:c.2623C>T
(TONSL)
|
NP_038460.4:p.Arg875Ter
|
|
NR_109770.1:n.273+370G>A
(TONSL-AS1)
|
|
|
ENST00000409379.7:c.2623C>T
(TONSL)
|
ENSP00000386239.3:p.Arg875Ter
|
|
ENST00000497613.2:n.3598C>T
(TONSL)
|
|
|
XM_011517047.1:c.2623C>T
(TONSL)
|
XP_011515349.1:p.Arg875Ter
|
|
XM_011517048.1:c.1651C>T
(TONSL)
|
XP_011515350.1:p.Arg551Ter
|
|
XM_011517048.2:c.1651C>T
(TONSL)
|
XP_011515350.1:p.Arg551Ter
|
|
XM_011517049.1:c.1615C>T
(TONSL)
|
XP_011515351.1:p.Arg539Ter
|
|
XM_011517049.2:c.1615C>T
(TONSL)
|
XP_011515351.1:p.Arg539Ter
|
|
XM_011517050.1:c.2623C>T
(TONSL)
|
XP_011515352.1:p.Arg875Ter
|
|
XM_011517050.2:c.2623C>T
(TONSL)
|
XP_011515352.1:p.Arg875Ter
|