ENST00000352909.8:c.100T>G
MANE Select
|
ENSP00000325951.4:p.Phe34Val
|
|
ENST00000324155.8:c.91-167T>G
|
ENSP00000325831.3:n.91-167T>G
|
|
ENST00000333684.9:c.100T>G
|
ENSP00000328814.6:p.Phe34Val
|
|
ENST00000352909.7:c.100T>G
|
ENSP00000325951.3:p.Phe34Val
|
|
ENST00000381168.7:c.103-167T>G
|
ENSP00000370560.3:n.103-167T>G
|
|
ENST00000381175.5:c.181T>G
|
ENSP00000370567.1:p.Phe61Val
|
|
ENST00000381178.5:c.193T>G
|
ENSP00000370571.1:p.Phe65Val
|
|
NM_000360.3:c.100T>G
|
NP_000351.2:p.Phe34Val
|
|
NM_199292.2:c.193T>G
|
NP_954986.2:p.Phe65Val
|
|
NM_199293.2:c.181T>G
|
NP_954987.2:p.Phe61Val
|
|
XM_011520335.1:c.112T>G
|
XP_011518637.1:p.Phe38Val
|
|
XM_011520335.2:c.112T>G
|
XP_011518637.1:p.Phe38Val
|
|
NM_000360.4:c.100T>G
MANE Select
|
NP_000351.2:p.Phe34Val
|
|
NM_199292.3:c.193T>G
|
NP_954986.2:p.Phe65Val
|
|
NM_199293.3:c.181T>G
|
NP_954987.2:p.Phe61Val
|
|