ENST00000389857.11:c.5124C>A
MANE Select
|
ENSP00000374507.6:p.Ala1708=
|
|
ENST00000331194.8:c.696C>A
|
ENSP00000330332.8:p.Ala232=
|
|
ENST00000334448.5:n.936C>A
|
|
|
ENST00000389857.10:c.5124C>A
|
ENSP00000374507.6:p.Ala1708=
|
|
ENST00000556726.5:c.1352C>A
|
|
|
NM_001080414.3:c.5124C>A
|
NP_001073883.2:p.Ala1708=
|
|
XM_011536796.1:c.5016C>A
|
XP_011535098.1:p.Ala1672=
|
|
XR_429316.2:n.5399C>A
|
|
|
XM_011536796.2:c.5016C>A
|
XP_011535098.1:p.Ala1672=
|
|
XM_017021336.1:c.2205C>A
|
XP_016876825.1:p.Ala735=
|
|
XR_429316.4:n.5397C>A
|
|
|
NM_001080414.4:c.5124C>A
MANE Select
|
NP_001073883.2:p.Ala1708=
|
|