ENST00000556489.4:c.*206G=
(PROX2)
MANE Select
|
ENSP00000451223.2:n.*206G=
|
|
ENST00000673765.1:c.*206G=
(PROX2)
|
ENSP00000501015.1:n.*206G=
|
|
ENST00000553381.1:n.238-291C=
(YLPM1)
|
|
|
ENST00000554107.2:c.206-291C=
(YLPM1)
|
|
|
ENST00000556084.6:c.1304G=
(PROX2)
|
ENSP00000451463.2:n.1304G=
|
|
ENST00000556489.3:c.1985G=
(PROX2)
|
ENSP00000451223.2:n.1985G=
|
|
NM_001080408.2:c.1304G=
(PROX2)
|
NP_001073877.2:n.1304G=
|
|
NM_001243007.1:c.1985G=
(PROX2)
|
NP_001229936.1:n.1985G=
|
|
XM_005267543.2:c.*206G=
(PROX2)
|
XP_005267600.1:n.*206G=
|
|
NM_001080408.3:c.*206G=
(PROX2)
|
NP_001073877.2:n.*206G=
|
|
NM_001243007.2:c.*206G=
(PROX2)
MANE Select
|
NP_001229936.1:n.*206G=
|
|
NM_001384314.1:c.*206G=
(PROX2)
|
NP_001371243.1:n.*206G=
|
|
NR_169190.1:n.2610G=
(PROX2)
|
|
|