ENST00000333213.11:c.*213T>C
MANE Select
|
ENSP00000327487.6:n.*213T>C
|
|
ENST00000434205.8:c.*213T>C
|
ENSP00000406559.4:n.*213T>C
|
|
ENST00000545228.3:c.*293T>C
|
ENSP00000438169.3:n.*293T>C
|
|
ENST00000577197.2:n.992T>C
|
|
|
ENST00000579449.2:n.2534T>C
|
|
|
ENST00000580013.6:n.2938T>C
|
|
|
ENST00000679370.1:n.3316T>C
|
|
|
ENST00000679429.1:c.*1252T>C
|
ENSP00000505403.1:n.*1252T>C
|
|
ENST00000679443.1:n.1863T>C
|
|
|
ENST00000679782.1:c.*493T>C
|
ENSP00000505995.1:n.*493T>C
|
|
ENST00000679919.1:n.2065T>C
|
|
|
ENST00000679928.1:c.*2346T>C
|
ENSP00000506071.1:n.*2346T>C
|
|
ENST00000680999.1:c.*213T>C
|
ENSP00000504984.1:n.*213T>C
|
|
ENST00000681282.1:c.*1981T>C
|
ENSP00000506339.1:n.*1981T>C
|
|
ENST00000333213.10:c.*213T>C
|
ENSP00000327487.6:n.*213T>C
|
|
ENST00000545228.2:c.1071T>C
|
|
|
ENST00000577197.1:n.542T>C
|
|
|
NM_207346.2:c.*213T>C
|
NP_997229.2:n.*213T>C
|
|
XM_005257229.2:c.*293T>C
|
XP_005257286.1:n.*293T>C
|
|
XM_006721821.2:c.*293T>C
|
XP_006721884.1:n.*293T>C
|
|
XM_011524616.1:c.*293T>C
|
XP_011522918.1:n.*293T>C
|
|
XM_011524618.1:c.*213T>C
|
XP_011522920.1:n.*213T>C
|
|
XR_243646.2:n.2026T>C
|
|
|
XM_005257229.4:c.*293T>C
|
XP_005257286.1:n.*293T>C
|
|
XR_243646.4:n.2032T>C
|
|
|
NM_207346.3:c.*213T>C
MANE Select
|
NP_997229.2:n.*213T>C
|
|