ENST00000315274.7:c.1246G>A
(MMP1)
MANE Select
|
ENSP00000322788.6:p.Ala416Thr
|
|
ENST00000680179.1:n.424G>A
(MMP1)
|
|
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ENST00000681445.1:n.420G>A
(MMP1)
|
|
|
ENST00000681643.1:n.446G>A
(MMP1)
|
|
|
ENST00000315274.6:c.1246G>A
(MMP1)
|
ENSP00000322788.6:p.Ala416Thr
|
|
ENST00000371455.7:n.325-7267C>T
(WTAPP1)
|
|
|
ENST00000525739.6:n.390-2388C>T
(WTAPP1)
|
|
|
ENST00000544704.1:n.344+6693C>T
(WTAPP1)
|
|
|
NM_001145938.1:c.1048G>A
(MMP1)
|
NP_001139410.1:p.Ala350Thr
|
|
NM_002421.3:c.1246G>A
(MMP1)
|
NP_002412.1:p.Ala416Thr
|
|
NR_038390.1:n.390-2388C>T
(WTAPP1)
|
|
|
NM_002421.4:c.1246G>A
(MMP1)
MANE Select
|
NP_002412.1:p.Ala416Thr
|
|
NM_001145938.2:c.1048G>A
(MMP1)
|
NP_001139410.1:p.Ala350Thr
|
|