ENST00000225964.10:c.4248G>T
MANE Select
|
ENSP00000225964.6:p.Thr1416=
|
|
ENST00000225964.9:c.4248G>T
|
ENSP00000225964.5:p.Thr1416=
|
|
NM_000088.3:c.4248G>T , LRG_1t1:c.4248G>T
|
NP_000079.2:p.Thr1416=
|
|
XM_005257058.3:c.3978G>T
|
XP_005257115.2:p.Thr1326=
|
|
XM_005257059.3:c.3330G>T
|
XP_005257116.2:p.Thr1110=
|
|
XM_011524341.1:c.4050G>T
|
XP_011522643.1:p.Thr1350=
|
|
XM_005257058.4:c.3978G>T
|
XP_005257115.2:p.Thr1326=
|
|
XM_005257059.4:c.3330G>T
|
XP_005257116.2:p.Thr1110=
|
|
NM_000088.4:c.4248G>T
MANE Select
|
NP_000079.2:p.Thr1416=
|
|