ENST00000225964.10:c.4301C>T
MANE Select
|
ENSP00000225964.6:p.Thr1434Ile
|
|
ENST00000225964.9:c.4301C>T
|
ENSP00000225964.5:p.Thr1434Ile
|
|
NM_000088.3:c.4301C>T , LRG_1t1:c.4301C>T
|
NP_000079.2:p.Thr1434Ile
|
|
XM_005257058.3:c.4031C>T
|
XP_005257115.2:p.Thr1344Ile
|
|
XM_005257059.3:c.3383C>T
|
XP_005257116.2:p.Thr1128Ile
|
|
XM_011524341.1:c.4103C>T
|
XP_011522643.1:p.Thr1368Ile
|
|
XM_005257058.4:c.4031C>T
|
XP_005257115.2:p.Thr1344Ile
|
|
XM_005257059.4:c.3383C>T
|
XP_005257116.2:p.Thr1128Ile
|
|
NM_000088.4:c.4301C>T
MANE Select
|
NP_000079.2:p.Thr1434Ile
|
|