|
ENST00000375687.10:c.347C>G
MANE Select
|
ENSP00000364839.4:p.Ala116Gly
|
|
|
ENST00000470145.3:n.290C>G
|
|
|
|
ENST00000643168.1:c.263C>G
|
ENSP00000495003.1:p.Ala88Gly
|
|
|
ENST00000644060.1:n.1151C>G
|
|
|
|
ENST00000644587.1:c.*186C>G
|
ENSP00000494813.1:n.*186C>G
|
|
|
ENST00000644615.1:n.51C>G
|
|
|
|
ENST00000645514.1:n.95C>G
|
|
|
|
ENST00000646985.1:c.317C>G
|
ENSP00000495053.1:p.Ala106Gly
|
|
|
ENST00000651418.1:c.347C>G
|
ENSP00000499150.1:p.Ala116Gly
|
|
|
ENST00000306058.9:c.332C>G
|
ENSP00000305119.5:p.Ala111Gly
|
|
|
ENST00000375687.8:c.347C>G
|
ENSP00000364839.4:p.Ala116Gly
|
|
|
ENST00000470145.2:n.290C>G
|
|
|
|
ENST00000613218.4:c.347C>G
|
ENSP00000480487.1:p.Ala116Gly
|
|
|
ENST00000620121.4:c.347C>G
|
ENSP00000481978.1:p.Ala116Gly
|
|
|
NM_015338.5:c.347C>G , LRG_630t1:c.347C>G
|
NP_056153.2:p.Ala116Gly
|
|
|
XM_006723727.2:c.344C>G
|
XP_006723790.1:p.Ala115Gly
|
|
|
XM_006723728.2:c.317C>G
|
XP_006723791.1:p.Ala106Gly
|
|
|
XM_006723730.2:c.263C>G
|
XP_006723793.1:p.Ala88Gly
|
|
|
XM_006723732.2:c.317C>G
|
XP_006723795.1:p.Ala106Gly
|
|
|
XM_011528647.1:c.611C>G
|
XP_011526949.1:p.Ala204Gly
|
|
|
XM_011528648.1:c.608C>G
|
XP_011526950.1:p.Ala203Gly
|
|
|
XM_011528649.1:c.527C>G
|
XP_011526951.1:p.Ala176Gly
|
|
|
XM_011528650.1:c.611C>G
|
XP_011526952.1:p.Ala204Gly
|
|
|
XM_011528651.1:c.326C>G
|
XP_011526953.1:p.Ala109Gly
|
|
|
XM_011528652.1:c.263C>G
|
XP_011526954.1:p.Ala88Gly
|
|
|
NM_001363734.1:c.317C>G
|
NP_001350663.1:p.Ala106Gly
|
|
|
XM_006723727.3:c.344C>G
|
XP_006723790.1:p.Ala115Gly
|
|
|
XM_006723728.3:c.317C>G
|
XP_006723791.1:p.Ala106Gly
|
|
|
XM_006723730.4:c.263C>G
|
XP_006723793.1:p.Ala88Gly
|
|
|
XM_011528648.3:c.608C>G
|
XP_011526950.1:p.Ala203Gly
|
|
|
XM_011528652.2:c.263C>G
|
XP_011526954.1:p.Ala88Gly
|
|
|
XM_017027704.1:c.263C>G
|
XP_016883193.1:p.Ala88Gly
|
|
|
XM_017027705.1:c.263C>G
|
XP_016883194.1:p.Ala88Gly
|
|
|
XM_017027706.1:c.347C>G
|
XP_016883195.1:p.Ala116Gly
|
|
|
NM_015338.6:c.347C>G
MANE Select
|
NP_056153.2:p.Ala116Gly
|
|
