ENST00000302328.9:c.2515T>G
MANE Select
|
ENSP00000307599.3:p.Phe839Val
|
|
ENST00000668754.1:c.2515T>G
|
ENSP00000499569.1:p.Phe839Val
|
|
ENST00000675223.1:c.2515T>G
|
ENSP00000502481.1:p.Phe839Val
|
|
ENST00000675672.1:c.2515T>G
|
ENSP00000502446.1:p.Phe839Val
|
|
ENST00000675892.1:c.2335T>G
|
ENSP00000502318.1:p.Phe779Val
|
|
ENST00000676045.1:c.2559T>G
|
ENSP00000501685.1:n.2559T>G
|
|
ENST00000676176.1:c.2134T>G
|
ENSP00000501891.1:p.Phe712Val
|
|
ENST00000302328.7:c.2515T>G
|
ENSP00000307599.3:p.Phe839Val
|
|
ENST00000444237.2:c.2515T>G
|
ENSP00000408028.2:p.Phe839Val
|
|
ENST00000456224.7:c.2515T>G
|
ENSP00000416757.3:p.Phe839Val
|
|
NM_001287223.1:c.2515T>G
|
NP_001274152.1:p.Phe839Val
|
|
NM_014139.2:c.2515T>G
|
NP_054858.2:p.Phe839Val
|
|
XM_011533320.1:c.2515T>G
|
XP_011531622.1:p.Phe839Val
|
|
XM_011533321.1:c.1852T>G
|
XP_011531623.1:p.Phe618Val
|
|
XM_011533322.1:c.1063T>G
|
XP_011531624.1:p.Phe355Val
|
|
NM_001349253.1:c.2515T>G
|
NP_001336182.1:p.Phe839Val
|
|
XM_011533321.2:c.1852T>G
|
XP_011531623.1:p.Phe618Val
|
|
XM_017005647.1:c.2890T>G
|
XP_016861136.1:p.Phe964Val
|
|
XM_017005648.1:c.2317T>G
|
XP_016861137.1:p.Phe773Val
|
|
XM_017005650.1:c.2515T>G
|
XP_016861139.1:p.Phe839Val
|
|
XM_017005651.1:c.2242T>G
|
XP_016861140.1:p.Phe748Val
|
|
XM_017005652.1:c.2515T>G
|
XP_016861141.1:p.Phe839Val
|
|
XM_017005653.1:c.919T>G
|
XP_016861142.1:p.Phe307Val
|
|
NM_001349253.2:c.2515T>G
MANE Select
|
NP_001336182.1:p.Phe839Val
|
|
NM_014139.3:c.2515T>G
|
NP_054858.2:p.Phe839Val
|
|