ENST00000545712.7:c.583C>T
MANE Select
|
ENSP00000445920.1:p.Arg195Cys
|
|
ENST00000537496.5:c.*148C>T
|
ENSP00000444793.1:n.*148C>T
|
|
ENST00000540016.5:c.427C>T
|
ENSP00000474582.1:p.Arg143Cys
|
|
ENST00000541763.6:c.808C>T
|
ENSP00000474981.1:n.808C>T
|
|
ENST00000544051.5:c.*464C>T
|
ENSP00000438079.1:n.*464C>T
|
|
ENST00000545712.6:c.583C>T
|
ENSP00000445920.1:p.Arg195Cys
|
|
NM_052845.3:c.583C>T
|
NP_443077.1:p.Arg195Cys
|
|
NR_038118.1:n.743C>T
|
|
|
XM_011538266.1:c.428C>T
|
XP_011536568.1:p.Thr143Met
|
|
XM_011538267.1:c.428C>T
|
XP_011536569.1:p.Thr143Met
|
|
XM_011538268.1:c.310C>T
|
XP_011536570.1:p.Arg104Cys
|
|
XM_011538269.1:c.307C>T
|
XP_011536571.1:p.Arg103Cys
|
|
XM_011538267.3:c.428C>T
|
XP_011536569.1:p.Thr143Met
|
|
XM_011538268.2:c.310C>T
|
XP_011536570.1:p.Arg104Cys
|
|
XM_011538269.2:c.307C>T
|
XP_011536571.1:p.Arg103Cys
|
|
XM_024448961.1:c.583C>T
|
XP_024304729.1:p.Arg195Cys
|
|
NM_052845.4:c.583C>T
MANE Select
|
NP_443077.1:p.Arg195Cys
|
|
NR_038118.2:n.694C>T
|
|
|