ENST00000352909.8:c.631T>G
MANE Select
|
ENSP00000325951.4:p.Phe211Val
|
|
ENST00000324155.8:c.*320T>G
|
ENSP00000325831.3:n.*320T>G
|
|
ENST00000333684.9:c.631T>G
|
ENSP00000328814.6:p.Phe211Val
|
|
ENST00000352909.7:c.631T>G
|
ENSP00000325951.3:p.Phe211Val
|
|
ENST00000381168.7:c.*320T>G
|
ENSP00000370560.3:n.*320T>G
|
|
ENST00000381175.5:c.712T>G
|
ENSP00000370567.1:p.Phe238Val
|
|
ENST00000381178.5:c.724T>G
|
ENSP00000370571.1:p.Phe242Val
|
|
ENST00000412076.1:c.71T>G
|
|
|
ENST00000416223.5:c.71T>G
|
|
|
ENST00000469226.1:n.380T>G
|
|
|
NM_000360.3:c.631T>G
|
NP_000351.2:p.Phe211Val
|
|
NM_199292.2:c.724T>G
|
NP_954986.2:p.Phe242Val
|
|
NM_199293.2:c.712T>G
|
NP_954987.2:p.Phe238Val
|
|
XM_011520335.1:c.643T>G
|
XP_011518637.1:p.Phe215Val
|
|
XM_011520335.2:c.643T>G
|
XP_011518637.1:p.Phe215Val
|
|
NM_000360.4:c.631T>G
MANE Select
|
NP_000351.2:p.Phe211Val
|
|
NM_199292.3:c.724T>G
|
NP_954986.2:p.Phe242Val
|
|
NM_199293.3:c.712T>G
|
NP_954987.2:p.Phe238Val
|
|