ENST00000673913.2:c.*174G>C
|
ENSP00000501161.2:n.*174G>C
|
|
ENST00000710286.1:c.2191G>C
|
ENSP00000518176.1:p.Glu731Gln
|
|
ENST00000673903.1:c.1459G>C
|
ENSP00000501257.1:p.Glu487Gln
|
|
ENST00000673913.1:c.684G>C
|
ENSP00000501161.1:n.684G>C
|
|
ENST00000302118.5:c.1834G>C
MANE Select
|
ENSP00000303208.5:p.Glu612Gln
|
|
ENST00000490692.1:n.2380G>C
|
|
|
NM_174936.3:c.1834G>C , LRG_275t1:c.1834G>C
|
NP_777596.2:p.Glu612Gln
|
|
NR_110451.1:n.1441G>C
|
|
|
XM_011541193.1:c.955G>C
|
XP_011539495.1:p.Glu319Gln
|
|
NM_174936.4:c.1834G>C
MANE Select
|
NP_777596.2:p.Glu612Gln
|
|
NR_110451.2:n.1441G>C
|
|
|