ENST00000218099.7:c.1063G>C
MANE Select
|
ENSP00000218099.2:p.Gly355Arg
|
|
ENST00000643157.1:n.1723+7G>C
|
|
|
ENST00000218099.6:c.1063G>C
|
ENSP00000218099.2:p.Gly355Arg
|
|
ENST00000394090.2:c.949G>C
|
ENSP00000377650.2:p.Gly317Arg
|
|
NM_000133.3:c.1063G>C , LRG_556t1:c.1063G>C
|
NP_000124.1:p.Gly355Arg
|
|
NM_001313913.1:c.949G>C
|
NP_001300842.1:p.Gly317Arg
|
|
XM_005262397.3:c.934G>C
|
XP_005262454.1:p.Gly312Arg
|
|
XM_005262397.4:c.934G>C
|
XP_005262454.1:p.Gly312Arg
|
|
NM_000133.4:c.1063G>C
MANE Select
|
NP_000124.1:p.Gly355Arg
|
|
NM_001313913.2:c.949G>C
|
NP_001300842.1:p.Gly317Arg
|
|