ENST00000685286.1:c.1311G>T
|
ENSP00000509457.1:p.Glu437Asp
|
|
ENST00000685664.1:c.1311G>T
|
ENSP00000509121.1:p.Glu437Asp
|
|
ENST00000686381.1:c.1047G>T
|
ENSP00000509555.1:p.Glu349Asp
|
|
ENST00000687065.1:c.1047G>T
|
ENSP00000510408.1:p.Glu349Asp
|
|
ENST00000687394.1:n.1417G>T
|
|
|
ENST00000687647.1:c.1047G>T
|
ENSP00000509205.1:p.Glu349Asp
|
|
ENST00000688035.1:n.1726G>T
|
|
|
ENST00000690315.1:c.1212G>T
|
ENSP00000509834.1:p.Glu404Asp
|
|
ENST00000690373.1:n.1650G>T
|
|
|
ENST00000690379.1:n.1341G>T
|
|
|
ENST00000690824.1:c.1311G>T
|
ENSP00000510709.1:p.Glu437Asp
|
|
ENST00000691661.1:c.1323G>T
|
ENSP00000510185.1:p.Glu441Asp
|
|
ENST00000691862.1:c.1209G>T
|
ENSP00000509291.1:p.Glu403Asp
|
|
ENST00000692813.1:c.1311G>T
|
ENSP00000509080.1:p.Glu437Asp
|
|
ENST00000692972.1:c.1386G>T
|
ENSP00000510753.1:p.Glu462Asp
|
|
ENST00000693454.1:n.521G>T
|
|
|
ENST00000693602.1:n.1404G>T
|
|
|
ENST00000358951.7:c.1311G>T
MANE Select
|
ENSP00000351832.2:p.Glu437Asp
|
|
ENST00000358951.6:c.1311G>T
|
ENSP00000351832.2:p.Glu437Asp
|
|
ENST00000478976.1:n.292-819G>T
|
|
|
NM_012414.3:c.1311G>T
|
NP_036546.2:p.Glu437Asp
|
|
NM_012414.4:c.1311G>T
MANE Select
|
NP_036546.2:p.Glu437Asp
|
|