ENST00000355943.8:c.926T=
MANE Select
|
ENSP00000348211.3:p.Met309=
|
|
ENST00000355943.7:c.926T=
|
ENSP00000348211.3:p.Met309=
|
|
ENST00000447245.6:c.683T=
|
ENSP00000399717.2:p.Met228=
|
|
ENST00000502462.6:n.1242T=
|
|
|
ENST00000504098.1:c.488T=
|
ENSP00000425708.1:p.Met163=
|
|
ENST00000509432.1:c.287T=
|
ENSP00000426604.1:p.Met96=
|
|
ENST00000513706.2:n.2526T=
|
|
|
ENST00000513807.5:c.440T=
|
ENSP00000421134.1:p.Met147=
|
|
NM_001303249.1:c.683T=
|
NP_001290178.1:p.Met228=
|
|
NM_001303250.1:c.653T=
|
NP_001290179.1:p.Met218=
|
|
NM_138773.2:c.926T=
|
NP_620128.1:p.Met309=
|
|
NM_001303249.2:c.683T=
|
NP_001290178.1:p.Met228=
|
|
NM_001303250.2:c.653T=
|
NP_001290179.1:p.Met218=
|
|
NM_138773.3:c.926T=
|
NP_620128.1:p.Met309=
|
|
NR_138151.1:n.1200T=
|
|
|
NM_138773.4:c.926T=
MANE Select
|
NP_620128.1:p.Met309=
|
|
NM_001303249.3:c.683T=
|
NP_001290178.1:p.Met228=
|
|
NM_001303250.3:c.653T=
|
NP_001290179.1:p.Met218=
|
|
NR_138151.2:n.1165T=
|
|
|