ENST00000315274.7:c.*449G>T
(MMP1)
MANE Select
|
ENSP00000322788.6:n.*449G>T
|
|
ENST00000680179.1:n.1037G>T
(MMP1)
|
|
|
ENST00000681445.1:n.1033G>T
(MMP1)
|
|
|
ENST00000681643.1:n.1059G>T
(MMP1)
|
|
|
ENST00000315274.6:c.*449G>T
(MMP1)
|
ENSP00000322788.6:n.*449G>T
|
|
ENST00000371455.7:n.325-8061C>A
(WTAPP1)
|
|
|
ENST00000525739.6:n.390-3182C>A
(WTAPP1)
|
|
|
ENST00000544704.1:n.344+5899C>A
(WTAPP1)
|
|
|
NM_001145938.1:c.*449G>T
(MMP1)
|
NP_001139410.1:n.*449G>T
|
|
NM_002421.3:c.*449G>T
(MMP1)
|
NP_002412.1:n.*449G>T
|
|
NR_038390.1:n.390-3182C>A
(WTAPP1)
|
|
|
NM_002421.4:c.*449G>T
(MMP1)
MANE Select
|
NP_002412.1:n.*449G>T
|
|
NM_001145938.2:c.*449G>T
(MMP1)
|
NP_001139410.1:n.*449G>T
|
|