ENST00000398603.6:c.437G>T
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ENSP00000381604.1:p.Gly146Val
|
|
ENST00000398606.10:c.545G>T
MANE Select
|
ENSP00000381607.3:p.Gly182Val
|
|
ENST00000646888.1:c.*261G>T
|
ENSP00000494477.1:n.*261G>T
|
|
ENST00000398603.5:c.437G>T
|
ENSP00000381604.1:p.Gly146Val
|
|
ENST00000398606.7:c.545G>T
|
ENSP00000381607.3:p.Gly182Val
|
|
ENST00000467591.1:n.656G>T
|
|
|
ENST00000494593.1:n.1517G>T
|
|
|
ENST00000498765.5:c.608G>T
|
|
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NM_000852.3:c.545G>T , LRG_723t1:c.545G>T
|
NP_000843.1:p.Gly182Val
|
|
NM_000852.4:c.545G>T
MANE Select
|
NP_000843.1:p.Gly182Val
|
|