ENST00000302328.9:c.2624C>T
MANE Select
|
ENSP00000307599.3:p.Ala875Val
|
|
ENST00000668754.1:c.2624C>T
|
ENSP00000499569.1:p.Ala875Val
|
|
ENST00000675223.1:c.2624C>T
|
ENSP00000502481.1:p.Ala875Val
|
|
ENST00000675672.1:c.2624C>T
|
ENSP00000502446.1:p.Ala875Val
|
|
ENST00000675892.1:c.2444C>T
|
ENSP00000502318.1:p.Ala815Val
|
|
ENST00000676045.1:c.2668C>T
|
ENSP00000501685.1:n.2668C>T
|
|
ENST00000676176.1:c.2243C>T
|
ENSP00000501891.1:p.Ala748Val
|
|
ENST00000302328.7:c.2624C>T
|
ENSP00000307599.3:p.Ala875Val
|
|
ENST00000444237.2:c.2624C>T
|
ENSP00000408028.2:p.Ala875Val
|
|
ENST00000456224.7:c.2624C>T
|
ENSP00000416757.3:p.Ala875Val
|
|
NM_001287223.1:c.2624C>T
|
NP_001274152.1:p.Ala875Val
|
|
NM_014139.2:c.2624C>T
|
NP_054858.2:p.Ala875Val
|
|
XM_011533320.1:c.2624C>T
|
XP_011531622.1:p.Ala875Val
|
|
XM_011533321.1:c.1961C>T
|
XP_011531623.1:p.Ala654Val
|
|
XM_011533322.1:c.1172C>T
|
XP_011531624.1:p.Ala391Val
|
|
NM_001349253.1:c.2624C>T
|
NP_001336182.1:p.Ala875Val
|
|
XM_011533321.2:c.1961C>T
|
XP_011531623.1:p.Ala654Val
|
|
XM_017005647.1:c.2999C>T
|
XP_016861136.1:p.Ala1000Val
|
|
XM_017005648.1:c.2426C>T
|
XP_016861137.1:p.Ala809Val
|
|
XM_017005650.1:c.2624C>T
|
XP_016861139.1:p.Ala875Val
|
|
XM_017005651.1:c.2351C>T
|
XP_016861140.1:p.Ala784Val
|
|
XM_017005652.1:c.2624C>T
|
XP_016861141.1:p.Ala875Val
|
|
XM_017005653.1:c.1028C>T
|
XP_016861142.1:p.Ala343Val
|
|
NM_001349253.2:c.2624C>T
MANE Select
|
NP_001336182.1:p.Ala875Val
|
|
NM_014139.3:c.2624C>T
|
NP_054858.2:p.Ala875Val
|
|