ENST00000340855.11:c.882G>A
MANE Select
|
ENSP00000339801.6:p.Arg294=
|
|
ENST00000651111.1:c.249G>A
|
ENSP00000498395.1:p.Arg83=
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|
ENST00000340855.10:c.882G>A
|
ENSP00000339801.6:p.Arg294=
|
|
ENST00000370441.8:c.882G>A
|
ENSP00000359470.4:p.Arg294=
|
|
ENST00000422081.6:c.249G>A
|
ENSP00000477056.1:p.Arg83=
|
|
ENST00000441880.1:n.114-3340G>A
|
|
|
ENST00000464251.5:c.808G>A
|
ENSP00000428980.1:n.808G>A
|
|
ENST00000466323.5:c.*73G>A
|
ENSP00000418264.1:n.*73G>A
|
|
ENST00000490775.5:n.667G>A
|
|
|
NM_000202.6:c.882G>A
|
NP_000193.1:p.Arg294=
|
|
NM_001166550.2:c.612G>A
|
NP_001160022.1:p.Arg204=
|
|
NM_006123.4:c.882G>A
|
NP_006114.1:p.Arg294=
|
|
NR_104128.1:n.1229G>A
|
|
|
NM_000202.7:c.882G>A
|
NP_000193.1:p.Arg294=
|
|
NM_001166550.3:c.612G>A
|
NP_001160022.1:p.Arg204=
|
|
NM_000202.8:c.882G>A
MANE Select
|
NP_000193.1:p.Arg294=
|
|
NM_001166550.4:c.612G>A
|
NP_001160022.1:p.Arg204=
|
|
NM_006123.5:c.882G>A
|
NP_006114.1:p.Arg294=
|
|
NR_104128.2:n.1181G>A
|
|
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