|
ENST00000392017.9:c.910T>G
MANE Select
|
ENSP00000375872.4:p.Ser304Ala
|
|
|
ENST00000347464.9:c.421T>G
|
ENSP00000318259.6:p.Ser141Ala
|
|
|
ENST00000373525.9:c.478T>G
|
ENSP00000362625.5:p.Ser160Ala
|
|
|
ENST00000392017.8:c.910T>G
|
ENSP00000375872.4:p.Ser304Ala
|
|
|
ENST00000392018.1:c.961T>G
|
ENSP00000375873.1:p.Ser321Ala
|
|
|
ENST00000392020.8:c.853T>G
|
ENSP00000375875.4:p.Ser285Ala
|
|
|
ENST00000392021.7:c.*791T>G
|
ENSP00000375876.3:n.*791T>G
|
|
|
ENST00000419681.5:c.421T>G
|
ENSP00000398773.1:p.Ser141Ala
|
|
|
ENST00000444735.5:c.529T>G
|
ENSP00000409215.1:p.Ser177Ala
|
|
|
ENST00000474148.5:n.1705T>G
|
|
|
|
ENST00000479942.5:n.1056T>G
|
|
|
|
ENST00000492298.5:n.431T>G
|
|
|
|
ENST00000498620.5:n.417T>G
|
|
|
|
NM_001190266.1:c.658T>G
|
NP_001177195.1:p.Ser220Ala
|
|
|
NM_001190267.1:c.562T>G
|
NP_001177196.1:p.Ser188Ala
|
|
|
NM_017974.3:c.853T>G
|
NP_060444.3:p.Ser285Ala
|
|
|
NM_030803.6:c.910T>G
|
NP_110430.5:p.Ser304Ala
|
|
|
NM_198890.2:c.421T>G
|
NP_942593.2:p.Ser141Ala
|
|
|
XM_005246082.1:c.961T>G
|
XP_005246139.1:p.Ser321Ala
|
|
|
XM_005246084.1:c.529T>G
|
XP_005246141.1:p.Ser177Ala
|
|
|
XM_005246086.1:c.478T>G
|
XP_005246143.1:p.Ser160Ala
|
|
|
XM_006712608.1:c.709T>G
|
XP_006712671.1:p.Ser237Ala
|
|
|
XR_241242.1:n.1155T>G
|
|
|
|
NM_001363742.1:c.961T>G
|
NP_001350671.1:p.Ser321Ala
|
|
|
XM_005246084.2:c.529T>G
|
XP_005246141.1:p.Ser177Ala
|
|
|
XM_005246086.2:c.478T>G
|
XP_005246143.1:p.Ser160Ala
|
|
|
XM_006712608.3:c.709T>G
|
XP_006712671.1:p.Ser237Ala
|
|
|
XR_001738801.2:n.1091T>G
|
|
|
|
XR_241242.3:n.1142T>G
|
|
|
|
NM_030803.7:c.910T>G
MANE Select
|
NP_110430.5:p.Ser304Ala
|
|
|
NM_001190266.2:c.658T>G
|
NP_001177195.1:p.Ser220Ala
|
|
|
NM_001190267.2:c.562T>G
|
NP_001177196.1:p.Ser188Ala
|
|
|
NM_001363742.2:c.961T>G
|
NP_001350671.1:p.Ser321Ala
|
|
|
NM_017974.4:c.853T>G
|
NP_060444.3:p.Ser285Ala
|
|
|
NM_198890.3:c.421T>G
|
NP_942593.2:p.Ser141Ala
|
|
