ENST00000243964.7:c.2949C>A
MANE Select
|
ENSP00000243964.4:p.Pro983=
|
|
ENST00000243964.6:c.2949C>A
|
ENSP00000243964.3:p.Pro983=
|
|
ENST00000454036.6:c.3018C>A
|
ENSP00000387694.1:p.Pro1006=
|
|
ENST00000616201.4:c.1298-2253C>A
|
ENSP00000484585.1:n.1298-2253C>A
|
|
ENST00000616202.4:c.613-2078C>A
|
ENSP00000478369.1:n.613-2078C>A
|
|
ENST00000616933.4:c.*2267C>A
|
ENSP00000477569.1:n.*2267C>A
|
|
ENST00000626937.2:c.510-3196C>A
|
ENSP00000485953.1:n.510-3196C>A
|
|
ENST00000628413.1:n.465C>A
|
|
|
NM_001134771.1:c.3018C>A
|
NP_001128243.1:p.Pro1006=
|
|
NM_020708.4:c.2949C>A
|
NP_065759.1:p.Pro983=
|
|
XM_017027981.1:c.3018C>A
|
XP_016883470.1:p.Pro1006=
|
|
NM_001134771.2:c.3018C>A
|
NP_001128243.1:p.Pro1006=
|
|
NM_020708.5:c.2949C>A
MANE Select
|
NP_065759.1:p.Pro983=
|
|