ENST00000225964.10:c.4326G>T
MANE Select
|
ENSP00000225964.6:p.Val1442=
|
|
ENST00000225964.9:c.4326G>T
|
ENSP00000225964.5:p.Val1442=
|
|
NM_000088.3:c.4326G>T , LRG_1t1:c.4326G>T
|
NP_000079.2:p.Val1442=
|
|
XM_005257058.3:c.4056G>T
|
XP_005257115.2:p.Val1352=
|
|
XM_005257059.3:c.3408G>T
|
XP_005257116.2:p.Val1136=
|
|
XM_011524341.1:c.4128G>T
|
XP_011522643.1:p.Val1376=
|
|
XM_005257058.4:c.4056G>T
|
XP_005257115.2:p.Val1352=
|
|
XM_005257059.4:c.3408G>T
|
XP_005257116.2:p.Val1136=
|
|
NM_000088.4:c.4326G>T
MANE Select
|
NP_000079.2:p.Val1442=
|
|