ENST00000673913.2:c.*176G>C
|
ENSP00000501161.2:n.*176G>C
|
|
ENST00000710286.1:c.2193G>C
|
ENSP00000518176.1:p.Glu731Asp
|
|
ENST00000673903.1:c.1461G>C
|
ENSP00000501257.1:p.Glu487Asp
|
|
ENST00000673913.1:c.686G>C
|
ENSP00000501161.1:n.686G>C
|
|
ENST00000302118.5:c.1836G>C
MANE Select
|
ENSP00000303208.5:p.Glu612Asp
|
|
ENST00000490692.1:n.2382G>C
|
|
|
NM_174936.3:c.1836G>C , LRG_275t1:c.1836G>C
|
NP_777596.2:p.Glu612Asp
|
|
NR_110451.1:n.1443G>C
|
|
|
XM_011541193.1:c.957G>C
|
XP_011539495.1:p.Glu319Asp
|
|
NM_174936.4:c.1836G>C
MANE Select
|
NP_777596.2:p.Glu612Asp
|
|
NR_110451.2:n.1443G>C
|
|
|