|
ENST00000356839.10:c.1558A>T
MANE Select
|
ENSP00000349297.5:p.Ser520Cys
|
|
|
ENST00000322910.9:c.*1513A>T
|
ENSP00000325395.5:n.*1513A>T
|
|
|
ENST00000350303.9:c.1492A>T
|
ENSP00000344152.5:p.Ser498Cys
|
|
|
ENST00000356839.9:c.1558A>T
|
ENSP00000349297.5:p.Ser520Cys
|
|
|
ENST00000542255.6:c.416A>T
|
|
|
|
ENST00000543245.6:c.1627A>T
|
ENSP00000438689.2:p.Ser543Cys
|
|
|
ENST00000578319.5:n.53A>T
|
|
|
|
ENST00000578711.1:n.842A>T
|
|
|
|
ENST00000578809.5:n.130A>T
|
|
|
|
ENST00000579391.1:n.166A>T
|
|
|
|
ENST00000579425.5:n.674A>T
|
|
|
|
ENST00000579546.1:c.297A>T
|
|
|
|
ENST00000579894.5:n.345A>T
|
|
|
|
ENST00000582450.1:n.66A>T
|
|
|
|
ENST00000583074.5:n.179A>T
|
|
|
|
ENST00000583850.5:n.333A>T
|
|
|
|
ENST00000583858.5:c.489A>T
|
|
|
|
ENST00000585203.6:n.749A>T
|
|
|
|
NM_000018.3:c.1558A>T
|
NP_000009.1:p.Ser520Cys
|
|
|
NM_001033859.2:c.1492A>T
|
NP_001029031.1:p.Ser498Cys
|
|
|
NM_001270447.1:c.1627A>T
|
NP_001257376.1:p.Ser543Cys
|
|
|
NM_001270448.1:c.1330A>T
|
NP_001257377.1:p.Ser444Cys
|
|
|
XM_006721516.2:c.1558A>T
|
XP_006721579.2:p.Ser520Cys
|
|
|
XM_011523829.1:c.1460A>T
|
XP_011522131.1:p.Glu487Val
|
|
|
XM_011523830.1:c.1460A>T
|
XP_011522132.1:p.Glu487Val
|
|
|
XR_934021.1:n.1665A>T
|
|
|
|
XR_934022.1:n.1567A>T
|
|
|
|
XR_934023.1:n.1567A>T
|
|
|
|
XM_006721516.3:c.1558A>T
|
XP_006721579.2:p.Ser520Cys
|
|
|
XM_011523829.2:c.1460A>T
|
XP_011522131.1:p.Glu487Val
|
|
|
XM_011523830.2:c.1460A>T
|
XP_011522132.1:p.Glu487Val
|
|
|
XM_024450741.1:c.1460A>T
|
XP_024306509.1:p.Glu487Val
|
|
|
XR_934021.2:n.1617A>T
|
|
|
|
XR_934022.2:n.1519A>T
|
|
|
|
XR_934023.2:n.1519A>T
|
|
|
|
NM_000018.4:c.1558A>T
MANE Select
|
NP_000009.1:p.Ser520Cys
|
|
|
NM_001033859.3:c.1492A>T
|
NP_001029031.1:p.Ser498Cys
|
|
|
NM_001270447.2:c.1627A>T
|
NP_001257376.1:p.Ser543Cys
|
|
|
NM_001270448.2:c.1330A>T
|
NP_001257377.1:p.Ser444Cys
|
|
