ENST00000355943.8:c.1129A>G
MANE Select
|
ENSP00000348211.3:p.Arg377Gly
|
|
ENST00000355943.7:c.1129A>G
|
ENSP00000348211.3:p.Arg377Gly
|
|
ENST00000447245.6:c.886A>G
|
ENSP00000399717.2:p.Arg296Gly
|
|
ENST00000502462.6:n.1445A>G
|
|
|
ENST00000504098.1:c.691A>G
|
ENSP00000425708.1:p.Arg231Gly
|
|
ENST00000509432.1:c.490A>G
|
ENSP00000426604.1:p.Arg164Gly
|
|
ENST00000513706.2:n.2729A>G
|
|
|
ENST00000513807.5:c.643A>G
|
ENSP00000421134.1:p.Arg215Gly
|
|
NM_001303249.1:c.886A>G
|
NP_001290178.1:p.Arg296Gly
|
|
NM_001303250.1:c.856A>G
|
NP_001290179.1:p.Arg286Gly
|
|
NM_138773.2:c.1129A>G
|
NP_620128.1:p.Arg377Gly
|
|
NM_001303249.2:c.886A>G
|
NP_001290178.1:p.Arg296Gly
|
|
NM_001303250.2:c.856A>G
|
NP_001290179.1:p.Arg286Gly
|
|
NM_138773.3:c.1129A>G
|
NP_620128.1:p.Arg377Gly
|
|
NR_138151.1:n.1403A>G
|
|
|
NM_138773.4:c.1129A>G
MANE Select
|
NP_620128.1:p.Arg377Gly
|
|
NM_001303249.3:c.886A>G
|
NP_001290178.1:p.Arg296Gly
|
|
NM_001303250.3:c.856A>G
|
NP_001290179.1:p.Arg286Gly
|
|
NR_138151.2:n.1368A>G
|
|
|