|
ENST00000356839.10:c.539C>T
MANE Select
|
ENSP00000349297.5:p.Ala180Val
|
|
|
ENST00000322910.9:c.*494C>T
|
ENSP00000325395.5:n.*494C>T
|
|
|
ENST00000350303.9:c.473C>T
|
ENSP00000344152.5:p.Ala158Val
|
|
|
ENST00000356839.9:c.539C>T
|
ENSP00000349297.5:p.Ala180Val
|
|
|
ENST00000543245.6:c.608C>T
|
ENSP00000438689.2:p.Ala203Val
|
|
|
ENST00000577191.5:n.616C>T
|
|
|
|
ENST00000577433.5:n.747C>T
|
|
|
|
ENST00000577857.5:n.355C>T
|
|
|
|
ENST00000579286.5:n.720C>T
|
|
|
|
ENST00000579886.2:c.377C>T
|
ENSP00000463246.1:p.Ala126Val
|
|
|
ENST00000580365.1:n.270C>T
|
|
|
|
ENST00000581378.5:c.257C>T
|
|
|
|
ENST00000581562.5:n.525-353C>T
|
|
|
|
ENST00000582166.1:n.520C>T
|
|
|
|
ENST00000583312.5:c.539C>T
|
ENSP00000467920.1:p.Ala180Val
|
|
|
ENST00000583760.1:n.321C>T
|
|
|
|
NM_000018.3:c.539C>T
|
NP_000009.1:p.Ala180Val
|
|
|
NM_001033859.2:c.473C>T
|
NP_001029031.1:p.Ala158Val
|
|
|
NM_001270447.1:c.608C>T
|
NP_001257376.1:p.Ala203Val
|
|
|
NM_001270448.1:c.311C>T
|
NP_001257377.1:p.Ala104Val
|
|
|
XM_006721516.2:c.539C>T
|
XP_006721579.2:p.Ala180Val
|
|
|
XM_011523829.1:c.539C>T
|
XP_011522131.1:p.Ala180Val
|
|
|
XM_011523830.1:c.539C>T
|
XP_011522132.1:p.Ala180Val
|
|
|
XR_934021.1:n.646C>T
|
|
|
|
XR_934022.1:n.646C>T
|
|
|
|
XR_934023.1:n.646C>T
|
|
|
|
XM_006721516.3:c.539C>T
|
XP_006721579.2:p.Ala180Val
|
|
|
XM_011523829.2:c.539C>T
|
XP_011522131.1:p.Ala180Val
|
|
|
XM_011523830.2:c.539C>T
|
XP_011522132.1:p.Ala180Val
|
|
|
XM_024450741.1:c.539C>T
|
XP_024306509.1:p.Ala180Val
|
|
|
XR_934021.2:n.598C>T
|
|
|
|
XR_934022.2:n.598C>T
|
|
|
|
XR_934023.2:n.598C>T
|
|
|
|
NM_000018.4:c.539C>T
MANE Select
|
NP_000009.1:p.Ala180Val
|
|
|
NM_001033859.3:c.473C>T
|
NP_001029031.1:p.Ala158Val
|
|
|
NM_001270447.2:c.608C>T
|
NP_001257376.1:p.Ala203Val
|
|
|
NM_001270448.2:c.311C>T
|
NP_001257377.1:p.Ala104Val
|
|
