|
ENST00000375687.10:c.3676C>G
MANE Select
|
ENSP00000364839.4:p.Leu1226Val
|
|
|
ENST00000646985.1:c.3493C>G
|
ENSP00000495053.1:p.Leu1165Val
|
|
|
ENST00000647223.1:n.6029C>G
|
|
|
|
ENST00000651418.1:c.1869+1807C>G
|
ENSP00000499150.1:n.1869+1807C>G
|
|
|
ENST00000306058.9:c.3661C>G
|
ENSP00000305119.5:p.Leu1221Val
|
|
|
ENST00000375687.8:c.3676C>G
|
ENSP00000364839.4:p.Leu1226Val
|
|
|
ENST00000613218.4:c.3676C>G
|
ENSP00000480487.1:p.Leu1226Val
|
|
|
ENST00000620121.4:c.3676C>G
|
ENSP00000481978.1:p.Leu1226Val
|
|
|
NM_015338.5:c.3676C>G , LRG_630t1:c.3676C>G
|
NP_056153.2:p.Leu1226Val
|
|
|
XM_006723727.2:c.3673C>G
|
XP_006723790.1:p.Leu1225Val
|
|
|
XM_006723728.2:c.3646C>G
|
XP_006723791.1:p.Leu1216Val
|
|
|
XM_006723730.2:c.3592C>G
|
XP_006723793.1:p.Leu1198Val
|
|
|
XM_006723732.2:c.3493C>G
|
XP_006723795.1:p.Leu1165Val
|
|
|
XM_006723733.1:c.2992C>G
|
XP_006723796.1:p.Leu998Val
|
|
|
XM_011528647.1:c.3940C>G
|
XP_011526949.1:p.Leu1314Val
|
|
|
XM_011528648.1:c.3937C>G
|
XP_011526950.1:p.Leu1313Val
|
|
|
XM_011528649.1:c.3856C>G
|
XP_011526951.1:p.Leu1286Val
|
|
|
XM_011528650.1:c.3787C>G
|
XP_011526952.1:p.Leu1263Val
|
|
|
XM_011528651.1:c.3655C>G
|
XP_011526953.1:p.Leu1219Val
|
|
|
XM_011528652.1:c.3592C>G
|
XP_011526954.1:p.Leu1198Val
|
|
|
NM_001363734.1:c.3493C>G
|
NP_001350663.1:p.Leu1165Val
|
|
|
XM_006723727.3:c.3673C>G
|
XP_006723790.1:p.Leu1225Val
|
|
|
XM_006723728.3:c.3646C>G
|
XP_006723791.1:p.Leu1216Val
|
|
|
XM_006723730.4:c.3592C>G
|
XP_006723793.1:p.Leu1198Val
|
|
|
XM_011528648.3:c.3937C>G
|
XP_011526950.1:p.Leu1313Val
|
|
|
XM_011528652.2:c.3592C>G
|
XP_011526954.1:p.Leu1198Val
|
|
|
XM_017027704.1:c.3592C>G
|
XP_016883193.1:p.Leu1198Val
|
|
|
XM_017027705.1:c.3592C>G
|
XP_016883194.1:p.Leu1198Val
|
|
|
XM_017027706.1:c.3523C>G
|
XP_016883195.1:p.Leu1175Val
|
|
|
NM_015338.6:c.3676C>G
MANE Select
|
NP_056153.2:p.Leu1226Val
|
|
