ENST00000299314.12:c.502T>G
MANE Select
|
ENSP00000299314.7:p.Phe168Val
|
|
ENST00000299314.11:c.502T>G
|
ENSP00000299314.7:p.Phe168Val
|
|
ENST00000549940.5:c.502T>G
|
ENSP00000449150.1:p.Phe168Val
|
|
ENST00000550352.1:n.296T>G
|
|
|
ENST00000552681.1:c.136T>G
|
ENSP00000449217.1:p.Phe46Val
|
|
NM_024312.4:c.502T>G
|
NP_077288.2:p.Phe168Val
|
|
XM_006719593.2:c.502T>G
|
XP_006719656.1:p.Phe168Val
|
|
XM_011538731.1:c.421T>G
|
XP_011537033.1:p.Phe141Val
|
|
XM_006719593.3:c.502T>G
|
XP_006719656.1:p.Phe168Val
|
|
XM_011538731.2:c.421T>G
|
XP_011537033.1:p.Phe141Val
|
|
XM_017019961.1:c.286T>G
|
XP_016875450.1:p.Phe96Val
|
|
XM_017019962.2:c.-849T>G
|
XP_016875451.1:n.-849T>G
|
|
NM_024312.5:c.502T>G
MANE Select
|
NP_077288.2:p.Phe168Val
|
|