ENST00000389857.11:c.5202A>G
MANE Select
|
ENSP00000374507.6:p.Lys1734=
|
|
ENST00000331194.8:c.774A>G
|
ENSP00000330332.8:p.Lys258=
|
|
ENST00000334448.5:n.1014A>G
|
|
|
ENST00000389857.10:c.5202A>G
|
ENSP00000374507.6:p.Lys1734=
|
|
ENST00000556726.5:c.1430A>G
|
|
|
NM_001080414.3:c.5202A>G
|
NP_001073883.2:p.Lys1734=
|
|
XM_011536796.1:c.5094A>G
|
XP_011535098.1:p.Lys1698=
|
|
XR_429316.2:n.5477A>G
|
|
|
XM_011536796.2:c.5094A>G
|
XP_011535098.1:p.Lys1698=
|
|
XM_017021336.1:c.2283A>G
|
XP_016876825.1:p.Lys761=
|
|
XR_429316.4:n.5475A>G
|
|
|
NM_001080414.4:c.5202A>G
MANE Select
|
NP_001073883.2:p.Lys1734=
|
|