ENST00000502274.2:c.3302C>A
|
|
|
ENST00000515425.6:c.3406C>A
MANE Select
|
ENSP00000423660.1:p.Gln1136Lys
|
|
ENST00000675793.1:c.*2690C>A
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ENSP00000502039.1:n.*2690C>A
|
|
ENST00000323829.9:c.*2794C>A
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ENSP00000313025.5:n.*2794C>A
|
|
ENST00000504517.5:c.2936C>A
|
ENSP00000421779.1:n.2936C>A
|
|
ENST00000504690.5:c.3406C>A
|
ENSP00000425627.1:p.Gln1136Lys
|
|
ENST00000510779.1:c.2456C>A
|
|
|
ENST00000512049.5:c.3385C>A
|
ENSP00000421860.1:p.Gln1129Lys
|
|
ENST00000515229.5:n.68C>A
|
|
|
ENST00000515425.5:c.3406C>A
|
ENSP00000423660.1:p.Gln1136Lys
|
|
NM_024577.3:c.3406C>A , LRG_269t1:c.3406C>A
|
NP_078853.2:p.Gln1136Lys
|
|
NM_024577.4:c.3406C>A
MANE Select
|
NP_078853.2:p.Gln1136Lys
|
|