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NM_020975.6:c.1375G>A
MANE Select
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NP_066124.1:p.Glu459Lys
|
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ENST00000355710.8:c.1375G>A
MANE Select
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ENSP00000347942.3:p.Glu459Lys
|
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NM_001355216.1:c.613G>A
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NP_001342145.1:p.Glu205Lys
|
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NM_020630.4:c.1375G>A , LRG_518t2:c.1375G>A
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NP_065681.1:p.Glu459Lys
|
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NM_020630.5:c.1375G>A
|
NP_065681.1:p.Glu459Lys
|
|
NM_020630.6:c.1375G>A
|
NP_065681.1:p.Glu459Lys
|
|
NM_020975.4:c.1375G>A , LRG_518t1:c.1375G>A
|
NP_066124.1:p.Glu459Lys
|
|
NM_020975.5:c.1375G>A
|
NP_066124.1:p.Glu459Lys
|
|
ENST00000340058.5:c.1375G>A
|
ENSP00000344798.4:p.Glu459Lys
|
|
ENST00000340058.6:c.1375G>A
|
ENSP00000344798.4:p.Glu459Lys
|
|
ENST00000355710.7:c.1375G>A
|
ENSP00000347942.3:p.Glu459Lys
|
|
ENST00000498820.5:c.74-781G>A
|
ENSP00000419080.1:n.74-781G>A
|
|
ENST00000615310.4:c.1289+86G>A
|
ENSP00000480088.1:n.1289+86G>A
|
|
ENST00000615310.5:c.979G>A
|
ENSP00000480088.2:p.Glu327Lys
|
|
ENST00000671844.1:c.737G>A
|
ENSP00000500541.1:p.Arg246Gln
|
|
ENST00000672389.1:c.185G>A
|
ENSP00000500252.1:p.Arg62Gln
|
|
ENST00000683007.1:n.949G>A
|
|
|
ENST00000683872.1:n.136G>A
|
|
|
XM_011540027.1:c.1375G>A
|
XP_011538329.1:p.Glu459Lys
|