ENST00000333213.11:c.*162G>T
MANE Select
|
ENSP00000327487.6:n.*162G>T
|
|
ENST00000434205.8:c.*162G>T
|
ENSP00000406559.4:n.*162G>T
|
|
ENST00000545228.3:c.*242G>T
|
ENSP00000438169.3:n.*242G>T
|
|
ENST00000577197.2:n.941G>T
|
|
|
ENST00000579449.2:n.2483G>T
|
|
|
ENST00000580013.6:n.2887G>T
|
|
|
ENST00000679370.1:n.3265G>T
|
|
|
ENST00000679429.1:c.*1201G>T
|
ENSP00000505403.1:n.*1201G>T
|
|
ENST00000679443.1:n.1812G>T
|
|
|
ENST00000679782.1:c.*442G>T
|
ENSP00000505995.1:n.*442G>T
|
|
ENST00000679919.1:n.2014G>T
|
|
|
ENST00000679928.1:c.*2295G>T
|
ENSP00000506071.1:n.*2295G>T
|
|
ENST00000680999.1:c.*162G>T
|
ENSP00000504984.1:n.*162G>T
|
|
ENST00000681282.1:c.*1930G>T
|
ENSP00000506339.1:n.*1930G>T
|
|
ENST00000333213.10:c.*162G>T
|
ENSP00000327487.6:n.*162G>T
|
|
ENST00000545228.2:c.1020G>T
|
|
|
ENST00000577197.1:n.491G>T
|
|
|
NM_207346.2:c.*162G>T
|
NP_997229.2:n.*162G>T
|
|
XM_005257229.2:c.*242G>T
|
XP_005257286.1:n.*242G>T
|
|
XM_006721821.2:c.*242G>T
|
XP_006721884.1:n.*242G>T
|
|
XM_011524616.1:c.*242G>T
|
XP_011522918.1:n.*242G>T
|
|
XM_011524618.1:c.*162G>T
|
XP_011522920.1:n.*162G>T
|
|
XR_243646.2:n.1975G>T
|
|
|
XM_005257229.4:c.*242G>T
|
XP_005257286.1:n.*242G>T
|
|
XR_243646.4:n.1981G>T
|
|
|
NM_207346.3:c.*162G>T
MANE Select
|
NP_997229.2:n.*162G>T
|
|