ENST00000368666.7:c.168G>T
MANE Select
|
ENSP00000357655.4:p.Gln56His
|
|
ENST00000639360.1:c.72G>T
|
ENSP00000491774.1:p.Gln24His
|
|
ENST00000230529.9:c.168G>T
|
ENSP00000230529.5:p.Gln56His
|
|
ENST00000361714.5:c.168G>T
|
ENSP00000354734.2:p.Gln56His
|
|
ENST00000368663.4:c.168G>T
|
ENSP00000357652.4:p.Gln56His
|
|
ENST00000368664.7:c.222G>T
|
ENSP00000357653.3:p.Gln74His
|
|
ENST00000368666.6:c.222G>T
|
ENSP00000357655.3:p.Gln74His
|
|
ENST00000409166.5:c.-507-169G>T
|
ENSP00000386467.1:n.-507-169G>T
|
|
ENST00000454589.5:c.168G>T
|
ENSP00000395928.1:p.Gln56His
|
|
ENST00000604763.5:c.168G>T
|
ENSP00000473777.1:p.Gln56His
|
|
ENST00000620524.3:n.102G>T
|
|
|
NM_003880.3:c.168G>T
|
NP_003871.1:p.Gln56His
|
|
NM_198239.1:c.222G>T
|
NP_937882.1:p.Gln74His
|
|
NR_125353.1:n.358G>T
|
|
|
NR_125354.1:n.278G>T
|
|
|
XM_011536220.1:c.168G>T
|
XP_011534522.1:p.Gln56His
|
|
XM_011536221.1:c.231G>T
|
XP_011534523.1:p.Gln77His
|
|
XM_011536222.1:c.306G>T
|
XP_011534524.1:p.Gln102His
|
|
XM_011536222.2:c.231G>T
|
XP_011534524.2:p.Gln77His
|
|
XR_001743705.1:n.706G>T
|
|
|
NM_003880.4:c.168G>T
|
NP_003871.1:p.Gln56His
|
|
NM_198239.2:c.168G>T
MANE Select
|
NP_937882.2:p.Gln56His
|
|
NR_125353.2:n.422G>T
|
|
|
NR_125354.3:n.249G>T
|
|
|