ENST00000218099.7:c.891T>C
MANE Select
|
ENSP00000218099.2:p.Ile297=
|
|
ENST00000643157.1:n.1558T>C
|
|
|
ENST00000218099.6:c.891T>C
|
ENSP00000218099.2:p.Ile297=
|
|
ENST00000394090.2:c.777T>C
|
ENSP00000377650.2:p.Ile259=
|
|
NM_000133.3:c.891T>C , LRG_556t1:c.891T>C
|
NP_000124.1:p.Ile297=
|
|
NM_001313913.1:c.777T>C
|
NP_001300842.1:p.Ile259=
|
|
XM_005262397.3:c.762T>C
|
XP_005262454.1:p.Ile254=
|
|
XM_005262397.4:c.762T>C
|
XP_005262454.1:p.Ile254=
|
|
NM_000133.4:c.891T>C
MANE Select
|
NP_000124.1:p.Ile297=
|
|
NM_001313913.2:c.777T>C
|
NP_001300842.1:p.Ile259=
|
|