NM_000088.4:c.3258C>T
MANE Select
|
NP_000079.2:p.Pro1086=
|
ENST00000225964.10:c.3258C>T
MANE Select
|
ENSP00000225964.6:p.Pro1086=
|
NM_000088.3:c.3258C>T , LRG_1t1:c.3258C>T
|
NP_000079.2:p.Pro1086=
|
ENST00000225964.9:c.3258C>T
|
ENSP00000225964.5:p.Pro1086=
|
ENST00000486572.1:n.456C>T
|
|
ENST00000511732.1:n.582C>T
|
|
XM_005257058.3:c.2988C>T
|
XP_005257115.2:p.Pro996=
|
XM_005257058.4:c.2988C>T
|
XP_005257115.2:p.Pro996=
|
XM_005257059.3:c.2340C>T
|
XP_005257116.2:p.Pro780=
|
XM_005257059.4:c.2340C>T
|
XP_005257116.2:p.Pro780=
|
XM_011524341.1:c.3060C>T
|
XP_011522643.1:p.Pro1020=
|