ENST00000302068.9:c.1160C>G
MANE Select
|
ENSP00000306099.4:p.Ala387Gly
|
|
ENST00000302068.8:c.1160C>G
|
ENSP00000306099.4:p.Ala387Gly
|
|
ENST00000502545.5:n.939+408C>G
|
|
|
ENST00000509493.1:c.503C>G
|
ENSP00000426757.1:p.Ala168Gly
|
|
NM_001184741.1:c.983C>G
|
NP_001171670.1:p.Ala328Gly
|
|
NM_005141.4:c.1160C>G , LRG_558t1:c.1160C>G
|
NP_005132.2:p.Ala387Gly
|
|
NM_001382759.1:c.1028C>G
|
NP_001369688.1:p.Ala343Gly
|
|
NM_001382760.1:c.1160C>G
|
NP_001369689.1:p.Ala387Gly
|
|
NM_001382761.1:c.1160C>G
|
NP_001369690.1:p.Ala387Gly
|
|
NM_001382762.1:c.860C>G
|
NP_001369691.1:p.Ala287Gly
|
|
NM_001382763.1:c.1151C>G
|
NP_001369692.1:p.Ala384Gly
|
|
NM_001382764.1:c.1081-58C>G
|
NP_001369693.1:n.1081-58C>G
|
|
NM_001382765.1:c.1160C>G
|
NP_001369694.1:p.Ala387Gly
|
|
NM_005141.5:c.1160C>G
MANE Select
|
NP_005132.2:p.Ala387Gly
|
|