ENST00000477616.2:c.1259G>A
MANE Select
|
ENSP00000434241.1:p.Arg420His
|
|
ENST00000670667.1:c.1259G>A
|
ENSP00000499301.1:p.Arg420His
|
|
ENST00000376959.6:c.1259G>A
|
ENSP00000366158.2:p.Arg420His
|
|
ENST00000474951.1:c.-74-2910G>A
|
ENSP00000432438.1:n.-74-2910G>A
|
|
ENST00000477616.1:c.1259G>A
|
ENSP00000434241.1:p.Arg420His
|
|
NM_004977.2:c.1259G>A
|
NP_004968.2:p.Arg420His
|
|
NR_110912.1:n.48-2910G>A
|
|
|
XM_006723203.2:c.1259G>A
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XP_006723266.1:p.Arg420His
|
|
XM_011526925.1:c.1259G>A
|
XP_011525227.1:p.Arg420His
|
|
XM_011526926.1:c.1259G>A
|
XP_011525228.1:p.Arg420His
|
|
XM_011526927.1:c.1259G>A
|
XP_011525229.1:p.Arg420His
|
|
XM_011526928.1:c.1259G>A
|
XP_011525230.1:p.Arg420His
|
|
NM_001372305.1:c.1031G>A
|
NP_001359234.1:p.Arg344His
|
|
NM_004977.3:c.1259G>A
MANE Select
|
NP_004968.2:p.Arg420His
|
|
NR_110912.2:n.69-2910G>A
|
|
|