|
ENST00000356839.10:c.557T>A
MANE Select
|
ENSP00000349297.5:p.Phe186Tyr
|
|
|
ENST00000322910.9:c.*512T>A
|
ENSP00000325395.5:n.*512T>A
|
|
|
ENST00000350303.9:c.491T>A
|
ENSP00000344152.5:p.Phe164Tyr
|
|
|
ENST00000356839.9:c.557T>A
|
ENSP00000349297.5:p.Phe186Tyr
|
|
|
ENST00000543245.6:c.626T>A
|
ENSP00000438689.2:p.Phe209Tyr
|
|
|
ENST00000577191.5:n.634T>A
|
|
|
|
ENST00000577433.5:n.765T>A
|
|
|
|
ENST00000577857.5:n.373T>A
|
|
|
|
ENST00000579286.5:n.738T>A
|
|
|
|
ENST00000579886.2:c.395T>A
|
ENSP00000463246.1:p.Phe132Tyr
|
|
|
ENST00000580365.1:n.288T>A
|
|
|
|
ENST00000581378.5:c.275T>A
|
|
|
|
ENST00000581562.5:n.525-335T>A
|
|
|
|
ENST00000582166.1:n.538T>A
|
|
|
|
ENST00000583312.5:c.557T>A
|
ENSP00000467920.1:p.Phe186Tyr
|
|
|
ENST00000583760.1:n.339T>A
|
|
|
|
NM_000018.3:c.557T>A
|
NP_000009.1:p.Phe186Tyr
|
|
|
NM_001033859.2:c.491T>A
|
NP_001029031.1:p.Phe164Tyr
|
|
|
NM_001270447.1:c.626T>A
|
NP_001257376.1:p.Phe209Tyr
|
|
|
NM_001270448.1:c.329T>A
|
NP_001257377.1:p.Phe110Tyr
|
|
|
XM_006721516.2:c.557T>A
|
XP_006721579.2:p.Phe186Tyr
|
|
|
XM_011523829.1:c.557T>A
|
XP_011522131.1:p.Phe186Tyr
|
|
|
XM_011523830.1:c.557T>A
|
XP_011522132.1:p.Phe186Tyr
|
|
|
XR_934021.1:n.664T>A
|
|
|
|
XR_934022.1:n.664T>A
|
|
|
|
XR_934023.1:n.664T>A
|
|
|
|
XM_006721516.3:c.557T>A
|
XP_006721579.2:p.Phe186Tyr
|
|
|
XM_011523829.2:c.557T>A
|
XP_011522131.1:p.Phe186Tyr
|
|
|
XM_011523830.2:c.557T>A
|
XP_011522132.1:p.Phe186Tyr
|
|
|
XM_024450741.1:c.557T>A
|
XP_024306509.1:p.Phe186Tyr
|
|
|
XR_934021.2:n.616T>A
|
|
|
|
XR_934022.2:n.616T>A
|
|
|
|
XR_934023.2:n.616T>A
|
|
|
|
NM_000018.4:c.557T>A
MANE Select
|
NP_000009.1:p.Phe186Tyr
|
|
|
NM_001033859.3:c.491T>A
|
NP_001029031.1:p.Phe164Tyr
|
|
|
NM_001270447.2:c.626T>A
|
NP_001257376.1:p.Phe209Tyr
|
|
|
NM_001270448.2:c.329T>A
|
NP_001257377.1:p.Phe110Tyr
|
|
