ENST00000315757.9:c.1397C>T
MANE Select
|
ENSP00000327290.7:p.Thr466Ile
|
|
ENST00000315757.8:c.1397C>T
|
ENSP00000327290.7:p.Thr466Ile
|
|
ENST00000423218.6:c.1397C>T
|
ENSP00000403392.2:p.Thr466Ile
|
|
ENST00000566429.1:n.286C>T
|
|
|
ENST00000569346.5:n.376C>T
|
|
|
NM_001004439.1:c.1397C>T
|
NP_001004439.1:p.Thr466Ile
|
|
XM_005254228.2:c.1091C>T
|
XP_005254285.1:p.Thr364Ile
|
|
XM_011521363.1:c.1190C>T
|
XP_011519665.1:p.Thr397Ile
|
|
XM_005254228.3:c.1091C>T
|
XP_005254285.1:p.Thr364Ile
|
|
XM_011521363.2:c.1190C>T
|
XP_011519665.1:p.Thr397Ile
|
|
NM_001004439.2:c.1397C>T
MANE Select
|
NP_001004439.1:p.Thr466Ile
|
|