ENST00000682888.1:c.106T>G
|
ENSP00000508003.1:p.Phe36Val
|
|
ENST00000683162.1:c.106T>G
|
ENSP00000508059.1:p.Phe36Val
|
|
ENST00000683289.1:c.106T>G
|
ENSP00000508195.1:p.Phe36Val
|
|
ENST00000683917.1:n.336T>G
|
|
|
ENST00000684356.1:c.106T>G
|
ENSP00000507619.1:p.Phe36Val
|
|
ENST00000684745.1:n.1226T>G
|
|
|
ENST00000379374.5:c.1552T>G
MANE Select
|
ENSP00000368682.4:p.Phe518Val
|
|
ENST00000379374.4:c.1552T>G
|
ENSP00000368682.4:p.Phe518Val
|
|
NM_000444.5:c.1552T>G
|
NP_000435.3:p.Phe518Val
|
|
NM_001282754.1:c.1552T>G
|
NP_001269683.1:p.Phe518Val
|
|
XM_011545533.1:c.796T>G
|
XP_011543835.1:p.Phe266Val
|
|
XM_011545534.1:c.796T>G
|
XP_011543836.1:p.Phe266Val
|
|
XM_011545536.1:c.445T>G
|
XP_011543838.1:p.Phe149Val
|
|
XM_011545536.2:c.445T>G
|
XP_011543838.1:p.Phe149Val
|
|
XM_017029579.1:c.796T>G
|
XP_016885068.1:p.Phe266Val
|
|
XM_024452390.1:c.1261T>G
|
XP_024308158.1:p.Phe421Val
|
|
XR_001755695.1:n.2392T>G
|
|
|
NM_000444.6:c.1552T>G
MANE Select
|
NP_000435.3:p.Phe518Val
|
|
NM_001282754.2:c.1552T>G
|
NP_001269683.1:p.Phe518Val
|
|