ENST00000546609.2:n.635G>T
|
|
|
ENST00000713544.1:c.804G>T
|
ENSP00000518840.1:p.Trp268Cys
|
|
ENST00000713545.1:c.781G>T
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ENSP00000518841.1:p.Ala261Ser
|
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ENST00000228606.9:c.723G>T
MANE Select
|
ENSP00000228606.4:p.Trp241Cys
|
|
ENST00000228606.8:c.723G>T
|
ENSP00000228606.4:p.Trp241Cys
|
|
ENST00000546567.5:c.18G>T
|
ENSP00000449472.1:p.Trp6Cys
|
|
ENST00000546609.1:c.635G>T
|
|
|
ENST00000547344.5:n.862G>T
|
|
|
ENST00000547451.1:n.523G>T
|
|
|
NM_000785.3:c.723G>T
|
NP_000776.1:p.Trp241Cys
|
|
NM_000785.4:c.723G>T
MANE Select
|
NP_000776.1:p.Trp241Cys
|
|