ENST00000389857.11:c.4764A>G
MANE Select
|
ENSP00000374507.6:p.Leu1588=
|
|
ENST00000331194.8:c.336A>G
|
ENSP00000330332.8:p.Leu112=
|
|
ENST00000334448.5:n.576A>G
|
|
|
ENST00000389857.10:c.4764A>G
|
ENSP00000374507.6:p.Leu1588=
|
|
ENST00000556726.5:c.992A>G
|
|
|
ENST00000557455.1:n.736A>G
|
|
|
NM_001080414.3:c.4764A>G
|
NP_001073883.2:p.Leu1588=
|
|
XM_011536796.1:c.4656A>G
|
XP_011535098.1:p.Leu1552=
|
|
XR_429316.2:n.5039A>G
|
|
|
XM_011536796.2:c.4656A>G
|
XP_011535098.1:p.Leu1552=
|
|
XM_017021336.1:c.1845A>G
|
XP_016876825.1:p.Leu615=
|
|
XR_429316.4:n.5037A>G
|
|
|
NM_001080414.4:c.4764A>G
MANE Select
|
NP_001073883.2:p.Leu1588=
|
|