ENST00000691183.1:c.222G>T
|
ENSP00000509954.1:p.Leu74=
|
|
ENST00000378842.8:c.222G>T
MANE Select
|
ENSP00000368119.4:p.Leu74=
|
|
ENST00000378842.7:c.222G>T
|
ENSP00000368119.3:p.Leu74=
|
|
ENST00000450095.6:c.20G>T
|
ENSP00000401956.2:p.Cys7Phe
|
|
ENST00000465543.6:n.561G>T
|
|
|
ENST00000468099.2:n.262G>T
|
|
|
ENST00000472111.5:n.263G>T
|
|
|
ENST00000473506.6:c.222G>T
|
ENSP00000432839.2:p.Leu74=
|
|
ENST00000473529.5:n.269G>T
|
|
|
ENST00000485531.1:n.215G>T
|
|
|
ENST00000487381.5:n.248G>T
|
|
|
ENST00000489643.6:n.252G>T
|
|
|
ENST00000554085.5:c.222G>T
|
ENSP00000450419.1:p.Leu74=
|
|
ENST00000554139.5:n.275G>T
|
|
|
ENST00000554330.5:n.219G>T
|
|
|
ENST00000554550.5:c.222G>T
|
ENSP00000451435.1:p.Leu74=
|
|
ENST00000554638.5:n.246G>T
|
|
|
ENST00000554897.5:c.222G>T
|
ENSP00000450942.1:p.Leu74=
|
|
ENST00000554944.5:n.252G>T
|
|
|
ENST00000555020.5:n.252G>T
|
|
|
ENST00000555086.5:n.226G>T
|
|
|
ENST00000555214.5:n.231G>T
|
|
|
ENST00000556157.1:n.329G>T
|
|
|
ENST00000556244.1:c.106G>T
|
|
|
ENST00000556278.1:c.222G>T
|
ENSP00000451792.1:p.Leu74=
|
|
ENST00000556403.5:n.235G>T
|
|
|
ENST00000556494.5:n.254G>T
|
|
|
ENST00000557541.5:n.415G>T
|
|
|
ENST00000557706.5:n.336G>T
|
|
|
NM_000155.3:c.222G>T
|
NP_000146.2:p.Leu74=
|
|
NM_001258332.1:c.20G>T
|
NP_001245261.1:p.Cys7Phe
|
|
NM_000155.4:c.222G>T
MANE Select
|
NP_000146.2:p.Leu74=
|
|
NM_001258332.2:c.20G>T
|
NP_001245261.1:p.Cys7Phe
|
|