ENST00000295897.9:c.1701A>C
MANE Select
|
ENSP00000295897.4:p.Gln567His
|
|
ENST00000295897.8:c.1701A>C
|
ENSP00000295897.4:p.Gln567His
|
|
ENST00000401494.7:c.1356A>C
|
ENSP00000384695.3:p.Gln452His
|
|
ENST00000415165.6:c.1125A>C
|
ENSP00000401820.2:p.Gln375His
|
|
ENST00000476441.6:c.*980A>C
|
ENSP00000423727.1:n.*980A>C
|
|
ENST00000495173.1:n.9A>C
|
|
|
ENST00000503124.5:c.1251A>C
|
ENSP00000421027.1:p.Gln417His
|
|
ENST00000505649.5:n.1248A>C
|
|
|
ENST00000508932.5:n.175+100A>C
|
|
|
ENST00000509063.5:c.1701A>C
|
ENSP00000422784.1:p.Gln567His
|
|
ENST00000511370.1:c.1234A>C
|
|
|
ENST00000621085.4:c.1062A>C
|
ENSP00000483421.1:p.Gln354His
|
|
ENST00000621628.4:c.1062A>C
|
ENSP00000480485.1:p.Gln354His
|
|
NM_000477.5:c.1701A>C
|
NP_000468.1:p.Gln567His
|
|
NM_000477.6:c.1701A>C
|
NP_000468.1:p.Gln567His
|
|
NM_000477.7:c.1701A>C
MANE Select
|
NP_000468.1:p.Gln567His
|
|