ENST00000320330.8:c.*1978A=
(PAGR1)
MANE Select
|
ENSP00000326519.6:n.*1978A=
|
|
ENST00000357402.10:c.-36+1222A=
(MVP)
MANE Select
|
ENSP00000349977.5:n.-36+1222A=
|
|
ENST00000357402.9:c.-36+1222A=
(MVP)
|
ENSP00000349977.5:n.-36+1222A=
|
|
ENST00000395353.5:c.-77+1222A=
(MVP)
|
ENSP00000378760.1:n.-77+1222A=
|
|
ENST00000562285.1:c.402+1830A=
|
|
|
ENST00000562463.5:c.-36+1222A=
(MVP)
|
ENSP00000457734.1:n.-36+1222A=
|
|
ENST00000563096.1:n.45+1222A=
(MVP)
|
|
|
ENST00000563558.5:c.-77+1222A=
(MVP)
|
ENSP00000454825.1:n.-77+1222A=
|
|
ENST00000563915.5:c.-77+1222A=
(MVP)
|
ENSP00000455819.1:n.-77+1222A=
|
|
ENST00000565164.1:c.-36+359A=
(MVP)
|
ENSP00000454819.1:n.-36+359A=
|
|
ENST00000565830.5:n.34+1222A=
(MVP)
|
|
|
ENST00000566066.5:c.-228+1222A=
(MVP)
|
ENSP00000455186.1:n.-228+1222A=
|
|
ENST00000566859.5:c.-36+1222A=
(MVP)
|
ENSP00000455741.1:n.-36+1222A=
|
|
ENST00000569887.1:c.-36+1222A=
(MVP)
|
ENSP00000455532.1:n.-36+1222A=
|
|
ENST00000570234.5:c.-146+341A=
(MVP)
|
ENSP00000456291.1:n.-146+341A=
|
|
NM_005115.4:c.-36+1222A=
(MVP)
|
NP_005106.2:n.-36+1222A=
|
|
NM_017458.3:c.-77+1222A=
(MVP)
|
NP_059447.2:n.-77+1222A=
|
|
NM_024516.3:c.*1978A=
(PAGR1)
|
NP_078792.1:n.*1978A=
|
|
NM_005115.5:c.-36+1222A=
(MVP)
MANE Select
|
NP_005106.2:n.-36+1222A=
|
|
NM_024516.4:c.*1978A=
(PAGR1)
MANE Select
|
NP_078792.1:n.*1978A=
|
|