|
ENST00000356839.10:c.232T>G
MANE Select
|
ENSP00000349297.5:p.Phe78Val
|
|
|
ENST00000322910.9:c.*187T>G
|
ENSP00000325395.5:n.*187T>G
|
|
|
ENST00000350303.9:c.166T>G
|
ENSP00000344152.5:p.Phe56Val
|
|
|
ENST00000356839.9:c.232T>G
|
ENSP00000349297.5:p.Phe78Val
|
|
|
ENST00000543245.6:c.301T>G
|
ENSP00000438689.2:p.Phe101Val
|
|
|
ENST00000577191.5:n.309T>G
|
|
|
|
ENST00000577433.5:n.440T>G
|
|
|
|
ENST00000577857.5:n.229-135T>G
|
|
|
|
ENST00000578269.5:n.679T>G
|
|
|
|
ENST00000578421.1:n.440T>G
|
|
|
|
ENST00000579286.5:n.413T>G
|
|
|
|
ENST00000579886.2:c.201+105T>G
|
ENSP00000463246.1:n.201+105T>G
|
|
|
ENST00000580263.5:n.396T>G
|
|
|
|
ENST00000581562.5:n.279T>G
|
|
|
|
ENST00000582056.5:n.322T>G
|
|
|
|
ENST00000582166.1:n.120T>G
|
|
|
|
ENST00000582356.5:n.431T>G
|
|
|
|
ENST00000583312.5:c.232T>G
|
ENSP00000467920.1:p.Phe78Val
|
|
|
ENST00000584103.5:c.232T>G
|
ENSP00000465353.1:p.Phe78Val
|
|
|
NM_000018.3:c.232T>G
|
NP_000009.1:p.Phe78Val
|
|
|
NM_001033859.2:c.166T>G
|
NP_001029031.1:p.Phe56Val
|
|
|
NM_001270447.1:c.301T>G
|
NP_001257376.1:p.Phe101Val
|
|
|
NM_001270448.1:c.4T>G
|
NP_001257377.1:p.Phe2Val
|
|
|
XM_006721516.2:c.232T>G
|
XP_006721579.2:p.Phe78Val
|
|
|
XM_011523829.1:c.232T>G
|
XP_011522131.1:p.Phe78Val
|
|
|
XM_011523830.1:c.232T>G
|
XP_011522132.1:p.Phe78Val
|
|
|
XR_934021.1:n.339T>G
|
|
|
|
XR_934022.1:n.339T>G
|
|
|
|
XR_934023.1:n.339T>G
|
|
|
|
XM_006721516.3:c.232T>G
|
XP_006721579.2:p.Phe78Val
|
|
|
XM_011523829.2:c.232T>G
|
XP_011522131.1:p.Phe78Val
|
|
|
XM_011523830.2:c.232T>G
|
XP_011522132.1:p.Phe78Val
|
|
|
XM_024450741.1:c.232T>G
|
XP_024306509.1:p.Phe78Val
|
|
|
XR_934021.2:n.291T>G
|
|
|
|
XR_934022.2:n.291T>G
|
|
|
|
XR_934023.2:n.291T>G
|
|
|
|
NM_000018.4:c.232T>G
MANE Select
|
NP_000009.1:p.Phe78Val
|
|
|
NM_001033859.3:c.166T>G
|
NP_001029031.1:p.Phe56Val
|
|
|
NM_001270447.2:c.301T>G
|
NP_001257376.1:p.Phe101Val
|
|
|
NM_001270448.2:c.4T>G
|
NP_001257377.1:p.Phe2Val
|
|
