ENST00000262027.10:c.1613G>C
MANE Select
|
ENSP00000262027.5:p.Arg538Thr
|
|
ENST00000262027.9:c.1613G>C
|
ENSP00000262027.5:p.Arg538Thr
|
|
ENST00000447721.6:n.1255G>C
|
|
|
ENST00000537638.6:c.1613G>C
|
ENSP00000446168.2:p.Arg538Thr
|
|
ENST00000545888.6:c.*1114G>C
|
ENSP00000439307.2:n.*1114G>C
|
|
ENST00000546971.5:n.357G>C
|
|
|
ENST00000548630.1:n.174G>C
|
|
|
ENST00000548944.1:c.134-4414G>C
|
ENSP00000449071.1:n.134-4414G>C
|
|
ENST00000549048.1:n.146G>C
|
|
|
ENST00000628866.2:c.*1114G>C
|
ENSP00000486738.1:n.*1114G>C
|
|
NM_004990.3:c.1613G>C
|
NP_004981.2:p.Arg538Thr
|
|
XM_006719398.2:c.911G>C
|
XP_006719461.1:p.Arg304Thr
|
|
XM_011538353.1:c.1613G>C
|
XP_011536655.1:p.Arg538Thr
|
|
XM_006719398.4:c.911G>C
|
XP_006719461.1:p.Arg304Thr
|
|
XR_001748704.2:n.1636G>C
|
|
|
XR_002957327.1:n.1560G>C
|
|
|
NM_004990.4:c.1613G>C
MANE Select
|
NP_004981.2:p.Arg538Thr
|
|