ENST00000298596.11:c.1729G>C
MANE Select
|
ENSP00000298596.6:p.Asp577His
|
|
ENST00000642869.1:c.2065G>C
|
ENSP00000494558.1:p.Asp689His
|
|
ENST00000298596.10:c.1729G>C
|
ENSP00000298596.6:p.Asp577His
|
|
ENST00000399162.2:c.463+3415G>C
|
ENSP00000382115.2:n.463+3415G>C
|
|
ENST00000399165.8:c.663+1066G>C
|
ENSP00000382118.4:n.663+1066G>C
|
|
ENST00000399169.8:c.1729G>C
|
ENSP00000382121.4:p.Asp577His
|
|
NM_001130159.2:c.663+1066G>C
|
NP_001123631.1:n.663+1066G>C
|
|
NM_001130160.2:c.463+3415G>C
|
NP_001123632.1:n.463+3415G>C
|
|
NM_001130161.2:c.1729G>C
|
NP_001123633.1:p.Asp577His
|
|
NM_152709.4:c.1729G>C
|
NP_689922.3:p.Asp577His
|
|
XM_011539454.1:c.1399G>C
|
XP_011537756.1:p.Asp467His
|
|
XM_011539454.2:c.1399G>C
|
XP_011537756.1:p.Asp467His
|
|
NM_152709.5:c.1729G>C
MANE Select
|
NP_689922.3:p.Asp577His
|
|
NM_001130161.3:c.1729G>C
|
NP_001123633.1:p.Asp577His
|
|
NM_001130159.3:c.663+1066G>C
|
NP_001123631.1:n.663+1066G>C
|
|
NM_001130160.3:c.463+3415G>C
|
NP_001123632.1:n.463+3415G>C
|
|
NM_001130161.4:c.1729G>C
|
NP_001123633.1:p.Asp577His
|
|