ENST00000389857.11:c.5090G>C
MANE Select
|
ENSP00000374507.6:p.Ser1697Thr
|
|
ENST00000331194.8:c.662G>C
|
ENSP00000330332.8:p.Ser221Thr
|
|
ENST00000334448.5:n.902G>C
|
|
|
ENST00000389857.10:c.5090G>C
|
ENSP00000374507.6:p.Ser1697Thr
|
|
ENST00000556726.5:c.1318G>C
|
|
|
NM_001080414.3:c.5090G>C
|
NP_001073883.2:p.Ser1697Thr
|
|
XM_011536796.1:c.4982G>C
|
XP_011535098.1:p.Ser1661Thr
|
|
XR_429316.2:n.5365G>C
|
|
|
XM_011536796.2:c.4982G>C
|
XP_011535098.1:p.Ser1661Thr
|
|
XM_017021336.1:c.2171G>C
|
XP_016876825.1:p.Ser724Thr
|
|
XR_429316.4:n.5363G>C
|
|
|
NM_001080414.4:c.5090G>C
MANE Select
|
NP_001073883.2:p.Ser1697Thr
|
|