ENST00000218099.7:c.1268G>T
MANE Select
|
ENSP00000218099.2:p.Ser423Ile
|
|
ENST00000643157.1:n.1723+212G>T
|
|
|
ENST00000218099.6:c.1268G>T
|
ENSP00000218099.2:p.Ser423Ile
|
|
ENST00000394090.2:c.1154G>T
|
ENSP00000377650.2:p.Ser385Ile
|
|
NM_000133.3:c.1268G>T , LRG_556t1:c.1268G>T
|
NP_000124.1:p.Ser423Ile
|
|
NM_001313913.1:c.1154G>T
|
NP_001300842.1:p.Ser385Ile
|
|
XM_005262397.3:c.1139G>T
|
XP_005262454.1:p.Ser380Ile
|
|
XM_005262397.4:c.1139G>T
|
XP_005262454.1:p.Ser380Ile
|
|
NM_000133.4:c.1268G>T
MANE Select
|
NP_000124.1:p.Ser423Ile
|
|
NM_001313913.2:c.1154G>T
|
NP_001300842.1:p.Ser385Ile
|
|