ENST00000642683.1:c.690G>T
|
ENSP00000495376.1:p.Gln230His
|
|
ENST00000643672.1:c.687G>T
|
ENSP00000494532.1:p.Gln229His
|
|
ENST00000645280.1:c.684G>T
|
ENSP00000496690.1:p.Gln228His
|
|
ENST00000648579.1:c.*35G>T
|
ENSP00000497638.1:n.*35G>T
|
|
ENST00000650617.1:c.738G>T
MANE Select
|
ENSP00000497532.1:p.Gln246His
|
|
ENST00000273158.8:c.738G>T
|
ENSP00000273158.3:p.Gln246His
|
|
NM_017875.2:c.738G>T
|
NP_060345.2:p.Gln246His
|
|
XM_006713214.1:c.726G>T
|
XP_006713277.1:p.Gln242His
|
|
XM_011533869.1:c.720G>T
|
XP_011532171.1:p.Gln240His
|
|
XM_011533870.1:c.687G>T
|
XP_011532172.1:p.Gln229His
|
|
XM_011533871.1:c.558G>T
|
XP_011532173.1:p.Gln186His
|
|
NM_001354798.1:c.626-1876G>T
|
NP_001341727.1:n.626-1876G>T
|
|
NM_017875.4:c.738G>T
MANE Select
|
NP_060345.2:p.Gln246His
|
|
XM_006713214.2:c.726G>T
|
XP_006713277.1:p.Gln242His
|
|
XM_011533869.2:c.720G>T
|
XP_011532171.1:p.Gln240His
|
|
XM_024453611.1:c.684G>T
|
XP_024309379.1:p.Gln228His
|
|
NM_001354798.2:c.626-1876G>T
|
NP_001341727.1:n.626-1876G>T
|
|