ENST00000360538.7:c.4-177G>T
(TOPORS)
MANE Select
|
ENSP00000353735.2:n.4-177G>T
|
|
ENST00000453396.5:n.2C>A
(SMIM27)
|
|
|
ENST00000680198.1:c.4-177G>T
|
ENSP00000505143.1:n.4-177G>T
|
|
ENST00000681750.1:c.-239-177G>T
|
ENSP00000506413.1:n.-239-177G>T
|
|
ENST00000360538.6:c.4-177G>T
(TOPORS)
|
ENSP00000353735.2:n.4-177G>T
|
|
ENST00000379858.1:c.3+1289G>T
(TOPORS)
|
ENSP00000369187.1:n.3+1289G>T
|
|
NM_001195622.1:c.3+1289G>T
(TOPORS)
|
NP_001182551.1:n.3+1289G>T
|
|
NM_005802.4:c.4-177G>T
(TOPORS)
|
NP_005793.2:n.4-177G>T
|
|
NR_033991.1:n.2C>A
(SMIM27)
|
|
|
NM_001349118.1:c.-750C>A
(SMIM27)
|
NP_001336047.1:n.-750C>A
|
|
XM_024447368.1:c.152C>A
(SMIM27)
|
XP_024303136.1:p.Pro51His
|
|
NM_005802.5:c.4-177G>T
(TOPORS)
MANE Select
|
NP_005793.2:n.4-177G>T
|
|
NM_001195622.2:c.3+1289G>T
(TOPORS)
|
NP_001182551.1:n.3+1289G>T
|
|