ENST00000369538.4:c.1186G>T
|
ENSP00000358551.4:p.Gly396Trp
|
|
ENST00000520113.7:c.1198G>T
MANE Select
|
ENSP00000430075.3:p.Gly400Trp
|
|
ENST00000637080.1:c.981G>T
|
ENSP00000489753.1:n.981G>T
|
|
ENST00000639077.1:n.863G>T
|
|
|
ENST00000369538.3:c.1285G>T
|
ENSP00000358551.3:p.Gly429Trp
|
|
ENST00000520113.6:c.1297G>T
|
ENSP00000430075.2:p.Gly433Trp
|
|
NM_000036.2:c.1297G>T
|
NP_000027.2:p.Gly433Trp
|
|
NM_001172626.1:c.1285G>T
|
NP_001166097.1:p.Gly429Trp
|
|
NM_000036.3:c.1198G>T
MANE Select
|
NP_000027.3:p.Gly400Trp
|
|
NM_001172626.2:c.1186G>T
|
NP_001166097.2:p.Gly396Trp
|
|