ENST00000357578.8:c.585A>G
MANE Select
|
ENSP00000350191.3:p.Ile195Met
|
|
ENST00000672352.1:c.348A>G
|
ENSP00000500876.1:p.Ile116Met
|
|
ENST00000672557.1:c.503A>G
|
|
|
ENST00000672652.1:c.506A>G
|
|
|
ENST00000675422.1:n.1345A>G
|
|
|
ENST00000348925.2:c.585A>G
|
ENSP00000314649.3:p.Ile195Met
|
|
ENST00000357578.7:c.585A>G
|
ENSP00000350191.3:p.Ile195Met
|
|
ENST00000491546.5:c.501A>G
|
ENSP00000417687.1:p.Ile167Met
|
|
NM_001080.3:c.585A>G
MANE Select
|
NP_001071.1:p.Ile195Met
|
|
NM_170740.1:c.585A>G
|
NP_733936.1:p.Ile195Met
|
|
NM_001368954.1:c.585A>G
|
NP_001355883.1:p.Ile195Met
|
|