ENST00000261195.3:c.1061G>C
MANE Select
|
ENSP00000261195.2:p.Arg354Thr
|
|
ENST00000647960.1:c.*1063G>C
|
ENSP00000497202.1:n.*1063G>C
|
|
ENST00000648372.1:n.988G>C
|
|
|
ENST00000261195.2:c.1061G>C
|
ENSP00000261195.2:p.Arg354Thr
|
|
NM_021957.3:c.1061G>C
|
NP_068776.2:p.Arg354Thr
|
|
XM_005253352.1:c.1061G>C
|
XP_005253409.1:p.Arg354Thr
|
|
XM_005253354.2:c.842G>C
|
XP_005253411.1:p.Arg281Thr
|
|
XM_006719062.2:c.1061G>C
|
XP_006719125.1:p.Arg354Thr
|
|
XM_006719063.2:c.830G>C
|
XP_006719126.1:p.Arg277Thr
|
|
NM_021957.4:c.1061G>C
MANE Select
|
NP_068776.2:p.Arg354Thr
|
|
XM_006719063.3:c.830G>C
|
XP_006719126.1:p.Arg277Thr
|
|
XM_017019245.2:c.1061G>C
|
XP_016874734.1:p.Arg354Thr
|
|
XM_024448960.1:c.1061G>C
|
XP_024304728.1:p.Arg354Thr
|
|