ENST00000368666.7:c.883T>G
MANE Select
|
ENSP00000357655.4:p.Phe295Val
|
|
ENST00000639360.1:c.784T>G
|
ENSP00000491774.1:p.Phe262Val
|
|
ENST00000230529.9:c.883T>G
|
ENSP00000230529.5:p.Phe295Val
|
|
ENST00000361714.5:c.883T>G
|
ENSP00000354734.2:p.Phe295Val
|
|
ENST00000368663.4:c.*189T>G
|
ENSP00000357652.4:n.*189T>G
|
|
ENST00000368664.7:c.*287T>G
|
ENSP00000357653.3:n.*287T>G
|
|
ENST00000368666.6:c.937T>G
|
ENSP00000357655.3:p.Phe313Val
|
|
ENST00000409166.5:c.211T>G
|
ENSP00000386467.1:p.Phe71Val
|
|
ENST00000454589.5:c.*287T>G
|
ENSP00000395928.1:n.*287T>G
|
|
ENST00000604763.5:c.883T>G
|
ENSP00000473777.1:p.Phe295Val
|
|
ENST00000613648.1:n.718T>G
|
|
|
ENST00000620524.3:n.814T>G
|
|
|
NM_003880.3:c.883T>G
|
NP_003871.1:p.Phe295Val
|
|
NM_198239.1:c.937T>G
|
NP_937882.1:p.Phe313Val
|
|
NR_125353.1:n.1137T>G
|
|
|
NR_125354.1:n.1057T>G
|
|
|
XM_011536220.1:c.883T>G
|
XP_011534522.1:p.Phe295Val
|
|
XM_011536221.1:c.*287T>G
|
XP_011534523.1:n.*287T>G
|
|
XM_011536223.1:c.301T>G
|
XP_011534525.1:p.Phe101Val
|
|
XM_011536223.3:c.301T>G
|
XP_011534525.1:p.Phe101Val
|
|
XR_001743705.1:n.1485T>G
|
|
|
NM_003880.4:c.883T>G
|
NP_003871.1:p.Phe295Val
|
|
NM_198239.2:c.883T>G
MANE Select
|
NP_937882.2:p.Phe295Val
|
|
NR_125353.2:n.1201T>G
|
|
|
NR_125354.3:n.1028T>G
|
|
|