ENST00000333213.11:c.1438G>T
MANE Select
|
ENSP00000327487.6:p.Glu480Ter
|
|
ENST00000434205.8:c.1135G>T
|
ENSP00000406559.4:p.Glu379Ter
|
|
ENST00000545228.3:c.1626G>T
|
ENSP00000438169.3:p.Met542Ile
|
|
ENST00000577197.2:n.636G>T
|
|
|
ENST00000579449.2:n.2178G>T
|
|
|
ENST00000580013.6:n.2582G>T
|
|
|
ENST00000679370.1:n.2960G>T
|
|
|
ENST00000679429.1:c.*896G>T
|
ENSP00000505403.1:n.*896G>T
|
|
ENST00000679443.1:n.1507G>T
|
|
|
ENST00000679782.1:c.*137G>T
|
ENSP00000505995.1:n.*137G>T
|
|
ENST00000679919.1:n.1709G>T
|
|
|
ENST00000679928.1:c.*1990G>T
|
ENSP00000506071.1:n.*1990G>T
|
|
ENST00000680528.1:n.2404G>T
|
|
|
ENST00000680999.1:c.1651G>T
|
ENSP00000504984.1:p.Glu551Ter
|
|
ENST00000681282.1:c.*1625G>T
|
ENSP00000506339.1:n.*1625G>T
|
|
ENST00000333213.10:c.1438G>T
|
ENSP00000327487.6:p.Glu480Ter
|
|
ENST00000545228.2:c.715G>T
|
|
|
ENST00000577197.1:n.186G>T
|
|
|
ENST00000579449.1:n.635G>T
|
|
|
NM_207346.2:c.1438G>T
|
NP_997229.2:p.Glu480Ter
|
|
XM_005257229.2:c.1626G>T
|
XP_005257286.1:p.Met542Ile
|
|
XM_006721821.2:c.1323G>T
|
XP_006721884.1:p.Met441Ile
|
|
XM_011524616.1:c.1509G>T
|
XP_011522918.1:p.Met503Ile
|
|
XM_011524617.1:c.*20G>T
|
XP_011522919.1:n.*20G>T
|
|
XM_011524618.1:c.1321G>T
|
XP_011522920.1:p.Glu441Ter
|
|
XR_243646.2:n.1670G>T
|
|
|
XM_005257229.4:c.1626G>T
|
XP_005257286.1:p.Met542Ile
|
|
XR_001753015.1:n.87+42C>A
|
|
|
XR_001753016.1:n.88+42C>A
|
|
|
XR_243646.4:n.1676G>T
|
|
|
NM_207346.3:c.1438G>T
MANE Select
|
NP_997229.2:p.Glu480Ter
|
|