ENST00000556489.4:c.*214G=
(PROX2)
MANE Select
|
ENSP00000451223.2:n.*214G=
|
|
ENST00000673765.1:c.*214G=
(PROX2)
|
ENSP00000501015.1:n.*214G=
|
|
ENST00000553381.1:n.238-299C=
(YLPM1)
|
|
|
ENST00000554107.2:c.206-299C=
(YLPM1)
|
|
|
ENST00000556084.6:c.1312G=
(PROX2)
|
ENSP00000451463.2:n.1312G=
|
|
ENST00000556489.3:c.1993G=
(PROX2)
|
ENSP00000451223.2:n.1993G=
|
|
NM_001080408.2:c.1312G=
(PROX2)
|
NP_001073877.2:n.1312G=
|
|
NM_001243007.1:c.1993G=
(PROX2)
|
NP_001229936.1:n.1993G=
|
|
XM_005267543.2:c.*214G=
(PROX2)
|
XP_005267600.1:n.*214G=
|
|
NM_001080408.3:c.*214G=
(PROX2)
|
NP_001073877.2:n.*214G=
|
|
NM_001243007.2:c.*214G=
(PROX2)
MANE Select
|
NP_001229936.1:n.*214G=
|
|
NM_001384314.1:c.*214G=
(PROX2)
|
NP_001371243.1:n.*214G=
|
|
NR_169190.1:n.2618G=
(PROX2)
|
|
|