|
ENST00000347147.9:c.1099C>G
MANE Select
|
ENSP00000333355.6:p.Pro367Ala
|
|
|
ENST00000347147.8:c.1099C>G
|
ENSP00000333355.6:p.Pro367Ala
|
|
|
ENST00000381975.7:c.1095C>G
|
ENSP00000371402.3:p.Thr365=
|
|
|
ENST00000392432.6:c.1240C>G
|
ENSP00000376227.2:p.Pro414Ala
|
|
|
ENST00000419280.5:c.*395C>G
|
ENSP00000414077.1:n.*395C>G
|
|
|
ENST00000429560.1:c.291C>G
|
ENSP00000403053.1:p.Thr97=
|
|
|
ENST00000432352.5:c.373C>G
|
ENSP00000409963.1:p.Pro125Ala
|
|
|
ENST00000452358.5:c.598C>G
|
ENSP00000414333.1:p.Pro200Ala
|
|
|
ENST00000467284.1:n.145C>G
|
|
|
|
ENST00000473092.5:c.1099C>G
|
ENSP00000418674.1:p.Pro367Ala
|
|
|
ENST00000477651.5:n.863C>G
|
|
|
|
NM_001011655.2:c.1099C>G
|
NP_001011655.1:p.Pro367Ala
|
|
|
NM_001166305.1:c.1240C>G
|
NP_001159777.1:p.Pro414Ala
|
|
|
NM_001166306.1:c.1095C>G
|
NP_001159778.1:p.Thr365=
|
|
|
NM_138399.4:c.1099C>G
|
NP_612408.3:p.Pro367Ala
|
|
|
XM_005269371.3:c.1099C>G
|
XP_005269428.1:p.Pro367Ala
|
|
|
XM_011513318.1:c.1249C>G
|
XP_011511620.1:p.Pro417Ala
|
|
|
XM_011513319.1:c.1186C>G
|
XP_011511621.1:p.Pro396Ala
|
|
|
XM_011513320.1:c.1297C>G
|
XP_011511622.1:p.Pro433Ala
|
|
|
XM_011513321.1:c.1165C>G
|
XP_011511623.1:p.Pro389Ala
|
|
|
XM_011513322.1:c.1156C>G
|
XP_011511624.1:p.Pro386Ala
|
|
|
XM_011513323.1:c.994C>G
|
XP_011511625.1:p.Pro332Ala
|
|
|
XM_005269371.4:c.1099C>G
|
XP_005269428.1:p.Pro367Ala
|
|
|
XM_011513318.2:c.1249C>G
|
XP_011511620.1:p.Pro417Ala
|
|
|
XM_011513319.2:c.1186C>G
|
XP_011511621.1:p.Pro396Ala
|
|
|
XM_011513320.2:c.1297C>G
|
XP_011511622.1:p.Pro433Ala
|
|
|
XM_011513321.2:c.1165C>G
|
XP_011511623.1:p.Pro389Ala
|
|
|
XM_011513322.2:c.1156C>G
|
XP_011511624.1:p.Pro386Ala
|
|
|
XM_017007517.1:c.1108C>G
|
XP_016863006.1:p.Pro370Ala
|
|
|
XM_017007518.1:c.1108C>G
|
XP_016863007.1:p.Pro370Ala
|
|
|
NM_001011655.3:c.1099C>G
MANE Select
|
NP_001011655.1:p.Pro367Ala
|
|
|
NM_001166305.2:c.1240C>G
|
NP_001159777.1:p.Pro414Ala
|
|
|
NM_001166306.2:c.1095C>G
|
NP_001159778.1:p.Thr365=
|
|
|
NM_138399.5:c.1099C>G
|
NP_612408.3:p.Pro367Ala
|
|
