|
NM_001845.6:c.1076G>T
MANE Select
|
NP_001836.3:p.Gly359Val
|
|
ENST00000375820.10:c.1076G>T
MANE Select
|
ENSP00000364979.4:p.Gly359Val
|
|
NM_001303110.1:c.1076G>T
|
NP_001290039.1:p.Gly359Val
|
|
NM_001303110.2:c.1076G>T
|
NP_001290039.1:p.Gly359Val
|
|
NM_001845.5:c.1076G>T
|
NP_001836.3:p.Gly359Val
|
|
ENST00000375820.8:c.1076G>T
|
ENSP00000364979.4:p.Gly359Val
|
|
ENST00000543140.5:c.1076G>T
|
ENSP00000443348.1:p.Gly359Val
|
|
ENST00000543140.6:c.1076G>T
|
ENSP00000443348.1:p.Gly359Val
|
|
ENST00000647797.1:c.955G>T
|
|
|
ENST00000649738.1:n.1206G>T
|
|
|
XM_011521048.1:c.884G>T
|
XP_011519350.1:p.Gly295Val
|
|
XM_011521048.2:c.884G>T
|
XP_011519350.1:p.Gly295Val
|