|
ENST00000300762.2:c.-153+2004A>G
(MMP26)
|
ENSP00000300762.2:n.-153+2004A>G
|
|
|
ENST00000380390.6:c.-145+2004A>G
(MMP26)
MANE Select
|
ENSP00000369753.1:n.-145+2004A>G
|
|
|
ENST00000624103.2:c.594T>C
(OR51F1)
MANE Select
|
ENSP00000485387.2:p.Cys198=
|
|
|
ENST00000343430.3:c.573T>C
|
ENSP00000345163.3:p.Cys191=
|
|
|
ENST00000380383.1:c.594T>C
(OR51F1)
|
ENSP00000369744.1:p.Cys198=
|
|
|
ENST00000380390.5:c.-145+2004A>G
(MMP26)
|
ENSP00000369753.1:n.-145+2004A>G
|
|
|
ENST00000477339.5:n.191+2004A>G
(MMP26)
|
|
|
|
ENST00000624103.1:c.573T>C
(OR51F1)
|
ENSP00000485387.1:p.Cys191=
|
|
|
NM_001004752.1:c.573T>C
(OR51F1)
|
NP_001004752.1:p.Cys191=
|
|
|
NM_001004752.2:c.594T>C
(OR51F1)
MANE Select
|
NP_001004752.2:p.Cys198=
|
|
|
NM_001384608.1:c.-153+2004A>G
(MMP26)
|
NP_001371537.1:n.-153+2004A>G
|
|
|
NM_021801.5:c.-145+2004A>G
(MMP26)
MANE Select
|
NP_068573.2:n.-145+2004A>G
|
|
