ENST00000225964.10:c.4122G>T
MANE Select
|
ENSP00000225964.6:p.Val1374=
|
|
ENST00000225964.9:c.4122G>T
|
ENSP00000225964.5:p.Val1374=
|
|
ENST00000510710.3:n.1087G>T
|
|
|
NM_000088.3:c.4122G>T , LRG_1t1:c.4122G>T
|
NP_000079.2:p.Val1374=
|
|
XM_005257058.3:c.3852G>T
|
XP_005257115.2:p.Val1284=
|
|
XM_005257059.3:c.3204G>T
|
XP_005257116.2:p.Val1068=
|
|
XM_011524341.1:c.3924G>T
|
XP_011522643.1:p.Val1308=
|
|
XM_005257058.4:c.3852G>T
|
XP_005257115.2:p.Val1284=
|
|
XM_005257059.4:c.3204G>T
|
XP_005257116.2:p.Val1068=
|
|
NM_000088.4:c.4122G>T
MANE Select
|
NP_000079.2:p.Val1374=
|
|