ENST00000369538.4:c.500G>T
|
ENSP00000358551.4:p.Gly167Val
|
|
ENST00000520113.7:c.512G>T
MANE Select
|
ENSP00000430075.3:p.Gly171Val
|
|
ENST00000637080.1:c.515G>T
|
ENSP00000489753.1:p.Gly172Val
|
|
ENST00000639077.1:n.177G>T
|
|
|
ENST00000369538.3:c.599G>T
|
ENSP00000358551.3:p.Gly200Val
|
|
ENST00000485564.3:n.386G>T
|
|
|
ENST00000520113.6:c.611G>T
|
ENSP00000430075.2:p.Gly204Val
|
|
NM_000036.2:c.611G>T
|
NP_000027.2:p.Gly204Val
|
|
NM_001172626.1:c.599G>T
|
NP_001166097.1:p.Gly200Val
|
|
NM_000036.3:c.512G>T
MANE Select
|
NP_000027.3:p.Gly171Val
|
|
NM_001172626.2:c.500G>T
|
NP_001166097.2:p.Gly167Val
|
|