ENST00000615310.5:c.1445A>T
|
ENSP00000480088.2:p.Glu482Val
|
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ENST00000683007.1:n.1415A>T
|
|
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ENST00000683872.1:n.602A>T
|
|
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ENST00000340058.6:c.1841A>T
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ENSP00000344798.4:p.Glu614Val
|
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ENST00000355710.8:c.1841A>T
MANE Select
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ENSP00000347942.3:p.Glu614Val
|
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ENST00000671844.1:c.*435A>T
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ENSP00000500541.1:n.*435A>T
|
|
ENST00000672389.1:c.*435A>T
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ENSP00000500252.1:n.*435A>T
|
|
ENST00000340058.5:c.1841A>T
|
ENSP00000344798.4:p.Glu614Val
|
|
ENST00000355710.7:c.1841A>T
|
ENSP00000347942.3:p.Glu614Val
|
|
ENST00000498820.5:c.392A>T
|
ENSP00000419080.1:p.Glu131Val
|
|
ENST00000615310.4:c.1289+2405A>T
|
ENSP00000480088.1:n.1289+2405A>T
|
|
NM_020630.4:c.1841A>T , LRG_518t2:c.1841A>T
|
NP_065681.1:p.Glu614Val
|
|
NM_020975.4:c.1841A>T , LRG_518t1:c.1841A>T
|
NP_066124.1:p.Glu614Val
|
|
XM_011540027.1:c.1841A>T
|
XP_011538329.1:p.Glu614Val
|
|
NM_001355216.1:c.1079A>T
|
NP_001342145.1:p.Glu360Val
|
|
NM_020630.5:c.1841A>T
|
NP_065681.1:p.Glu614Val
|
|
NM_020975.5:c.1841A>T
|
NP_066124.1:p.Glu614Val
|
|
NM_020975.6:c.1841A>T
MANE Select
|
NP_066124.1:p.Glu614Val
|
|
NM_020630.6:c.1841A>T
|
NP_065681.1:p.Glu614Val
|
|