ENST00000642683.1:c.653T>G
|
ENSP00000495376.1:p.Val218Gly
|
|
ENST00000643672.1:c.650T>G
|
ENSP00000494532.1:p.Val217Gly
|
|
ENST00000645280.1:c.647T>G
|
ENSP00000496690.1:p.Val216Gly
|
|
ENST00000648579.1:c.757T>G
|
ENSP00000497638.1:p.Ter253Glu
|
|
ENST00000650617.1:c.701T>G
MANE Select
|
ENSP00000497532.1:p.Val234Gly
|
|
ENST00000273158.8:c.701T>G
|
ENSP00000273158.3:p.Val234Gly
|
|
NM_017875.2:c.701T>G
|
NP_060345.2:p.Val234Gly
|
|
XM_006713214.1:c.689T>G
|
XP_006713277.1:p.Val230Gly
|
|
XM_011533869.1:c.683T>G
|
XP_011532171.1:p.Val228Gly
|
|
XM_011533870.1:c.650T>G
|
XP_011532172.1:p.Val217Gly
|
|
XM_011533871.1:c.521T>G
|
XP_011532173.1:p.Val174Gly
|
|
NM_001354798.1:c.626-1913T>G
|
NP_001341727.1:n.626-1913T>G
|
|
NM_017875.4:c.701T>G
MANE Select
|
NP_060345.2:p.Val234Gly
|
|
XM_006713214.2:c.689T>G
|
XP_006713277.1:p.Val230Gly
|
|
XM_011533869.2:c.683T>G
|
XP_011532171.1:p.Val228Gly
|
|
XM_024453611.1:c.647T>G
|
XP_024309379.1:p.Val216Gly
|
|
NM_001354798.2:c.626-1913T>G
|
NP_001341727.1:n.626-1913T>G
|
|