ENST00000218099.7:c.1025C>G
MANE Select
|
ENSP00000218099.2:p.Thr342Arg
|
|
ENST00000643157.1:n.1692C>G
|
|
|
ENST00000218099.6:c.1025C>G
|
ENSP00000218099.2:p.Thr342Arg
|
|
ENST00000394090.2:c.911C>G
|
ENSP00000377650.2:p.Thr304Arg
|
|
NM_000133.3:c.1025C>G , LRG_556t1:c.1025C>G
|
NP_000124.1:p.Thr342Arg
|
|
NM_001313913.1:c.911C>G
|
NP_001300842.1:p.Thr304Arg
|
|
XM_005262397.3:c.896C>G
|
XP_005262454.1:p.Thr299Arg
|
|
XM_005262397.4:c.896C>G
|
XP_005262454.1:p.Thr299Arg
|
|
NM_000133.4:c.1025C>G
MANE Select
|
NP_000124.1:p.Thr342Arg
|
|
NM_001313913.2:c.911C>G
|
NP_001300842.1:p.Thr304Arg
|
|