ENST00000315274.7:c.1263A>G
(MMP1)
MANE Select
|
ENSP00000322788.6:p.Gly421=
|
|
ENST00000680179.1:n.441A>G
(MMP1)
|
|
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ENST00000681445.1:n.437A>G
(MMP1)
|
|
|
ENST00000681643.1:n.463A>G
(MMP1)
|
|
|
ENST00000315274.6:c.1263A>G
(MMP1)
|
ENSP00000322788.6:p.Gly421=
|
|
ENST00000371455.7:n.325-7284T>C
(WTAPP1)
|
|
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ENST00000525739.6:n.390-2405T>C
(WTAPP1)
|
|
|
ENST00000544704.1:n.344+6676T>C
(WTAPP1)
|
|
|
NM_001145938.1:c.1065A>G
(MMP1)
|
NP_001139410.1:p.Gly355=
|
|
NM_002421.3:c.1263A>G
(MMP1)
|
NP_002412.1:p.Gly421=
|
|
NR_038390.1:n.390-2405T>C
(WTAPP1)
|
|
|
NM_002421.4:c.1263A>G
(MMP1)
MANE Select
|
NP_002412.1:p.Gly421=
|
|
NM_001145938.2:c.1065A>G
(MMP1)
|
NP_001139410.1:p.Gly355=
|
|