ENST00000243964.7:c.2972A>T
MANE Select
|
ENSP00000243964.4:p.Glu991Val
|
|
ENST00000243964.6:c.2972A>T
|
ENSP00000243964.3:p.Glu991Val
|
|
ENST00000454036.6:c.3041A>T
|
ENSP00000387694.1:p.Glu1014Val
|
|
ENST00000616201.4:c.1298-2230A>T
|
ENSP00000484585.1:n.1298-2230A>T
|
|
ENST00000616202.4:c.613-2055A>T
|
ENSP00000478369.1:n.613-2055A>T
|
|
ENST00000616933.4:c.*2290A>T
|
ENSP00000477569.1:n.*2290A>T
|
|
ENST00000626937.2:c.510-3173A>T
|
ENSP00000485953.1:n.510-3173A>T
|
|
ENST00000628413.1:n.488A>T
|
|
|
NM_001134771.1:c.3041A>T
|
NP_001128243.1:p.Glu1014Val
|
|
NM_020708.4:c.2972A>T
|
NP_065759.1:p.Glu991Val
|
|
XM_017027981.1:c.3041A>T
|
XP_016883470.1:p.Glu1014Val
|
|
NM_001134771.2:c.3041A>T
|
NP_001128243.1:p.Glu1014Val
|
|
NM_020708.5:c.2972A>T
MANE Select
|
NP_065759.1:p.Glu991Val
|
|