ENST00000389857.11:c.4706G>A
MANE Select
|
ENSP00000374507.6:p.Arg1569Gln
|
|
ENST00000331194.8:c.278G>A
|
ENSP00000330332.8:p.Arg93Gln
|
|
ENST00000334448.5:n.518G>A
|
|
|
ENST00000389857.10:c.4706G>A
|
ENSP00000374507.6:p.Arg1569Gln
|
|
ENST00000556726.5:c.934G>A
|
|
|
ENST00000557455.1:n.678G>A
|
|
|
NM_001080414.3:c.4706G>A
|
NP_001073883.2:p.Arg1569Gln
|
|
XM_011536796.1:c.4598G>A
|
XP_011535098.1:p.Arg1533Gln
|
|
XR_429316.2:n.4981G>A
|
|
|
XM_011536796.2:c.4598G>A
|
XP_011535098.1:p.Arg1533Gln
|
|
XM_017021336.1:c.1787G>A
|
XP_016876825.1:p.Arg596Gln
|
|
XR_429316.4:n.4979G>A
|
|
|
NM_001080414.4:c.4706G>A
MANE Select
|
NP_001073883.2:p.Arg1569Gln
|
|