|
ENST00000392017.9:c.904C>G
MANE Select
|
ENSP00000375872.4:p.Pro302Ala
|
|
|
ENST00000347464.9:c.415C>G
|
ENSP00000318259.6:p.Pro139Ala
|
|
|
ENST00000373525.9:c.472C>G
|
ENSP00000362625.5:p.Pro158Ala
|
|
|
ENST00000392017.8:c.904C>G
|
ENSP00000375872.4:p.Pro302Ala
|
|
|
ENST00000392018.1:c.955C>G
|
ENSP00000375873.1:p.Pro319Ala
|
|
|
ENST00000392020.8:c.847C>G
|
ENSP00000375875.4:p.Pro283Ala
|
|
|
ENST00000392021.7:c.*785C>G
|
ENSP00000375876.3:n.*785C>G
|
|
|
ENST00000419681.5:c.415C>G
|
ENSP00000398773.1:p.Pro139Ala
|
|
|
ENST00000444735.5:c.523C>G
|
ENSP00000409215.1:p.Pro175Ala
|
|
|
ENST00000474148.5:n.1699C>G
|
|
|
|
ENST00000479942.5:n.1050C>G
|
|
|
|
ENST00000492298.5:n.425C>G
|
|
|
|
ENST00000498620.5:n.411C>G
|
|
|
|
NM_001190266.1:c.652C>G
|
NP_001177195.1:p.Pro218Ala
|
|
|
NM_001190267.1:c.556C>G
|
NP_001177196.1:p.Pro186Ala
|
|
|
NM_017974.3:c.847C>G
|
NP_060444.3:p.Pro283Ala
|
|
|
NM_030803.6:c.904C>G
|
NP_110430.5:p.Pro302Ala
|
|
|
NM_198890.2:c.415C>G
|
NP_942593.2:p.Pro139Ala
|
|
|
XM_005246082.1:c.955C>G
|
XP_005246139.1:p.Pro319Ala
|
|
|
XM_005246084.1:c.523C>G
|
XP_005246141.1:p.Pro175Ala
|
|
|
XM_005246086.1:c.472C>G
|
XP_005246143.1:p.Pro158Ala
|
|
|
XM_006712608.1:c.703C>G
|
XP_006712671.1:p.Pro235Ala
|
|
|
XR_241242.1:n.1149C>G
|
|
|
|
NM_001363742.1:c.955C>G
|
NP_001350671.1:p.Pro319Ala
|
|
|
XM_005246084.2:c.523C>G
|
XP_005246141.1:p.Pro175Ala
|
|
|
XM_005246086.2:c.472C>G
|
XP_005246143.1:p.Pro158Ala
|
|
|
XM_006712608.3:c.703C>G
|
XP_006712671.1:p.Pro235Ala
|
|
|
XR_001738801.2:n.1085C>G
|
|
|
|
XR_241242.3:n.1136C>G
|
|
|
|
NM_030803.7:c.904C>G
MANE Select
|
NP_110430.5:p.Pro302Ala
|
|
|
NM_001190266.2:c.652C>G
|
NP_001177195.1:p.Pro218Ala
|
|
|
NM_001190267.2:c.556C>G
|
NP_001177196.1:p.Pro186Ala
|
|
|
NM_001363742.2:c.955C>G
|
NP_001350671.1:p.Pro319Ala
|
|
|
NM_017974.4:c.847C>G
|
NP_060444.3:p.Pro283Ala
|
|
|
NM_198890.3:c.415C>G
|
NP_942593.2:p.Pro139Ala
|
|
