ENST00000218099.7:c.882A>C
MANE Select
|
ENSP00000218099.2:p.Arg294=
|
|
ENST00000643157.1:n.1549A>C
|
|
|
ENST00000218099.6:c.882A>C
|
ENSP00000218099.2:p.Arg294=
|
|
ENST00000394090.2:c.768A>C
|
ENSP00000377650.2:p.Arg256=
|
|
NM_000133.3:c.882A>C , LRG_556t1:c.882A>C
|
NP_000124.1:p.Arg294=
|
|
NM_001313913.1:c.768A>C
|
NP_001300842.1:p.Arg256=
|
|
XM_005262397.3:c.753A>C
|
XP_005262454.1:p.Arg251=
|
|
XM_005262397.4:c.753A>C
|
XP_005262454.1:p.Arg251=
|
|
NM_000133.4:c.882A>C
MANE Select
|
NP_000124.1:p.Arg294=
|
|
NM_001313913.2:c.768A>C
|
NP_001300842.1:p.Arg256=
|
|