ENST00000053867.8:c.1403A>G
MANE Select
|
ENSP00000053867.2:p.Gln468Arg
|
|
ENST00000639447.1:c.1137-291A>G
|
ENSP00000492014.1:n.1137-291A>G
|
|
ENST00000053867.7:c.1403A>G
|
ENSP00000053867.2:p.Gln468Arg
|
|
ENST00000586242.1:c.37A>G
|
|
|
ENST00000586443.1:c.844A>G
|
|
|
ENST00000589265.5:c.932A>G
|
ENSP00000467616.1:p.Gln311Arg
|
|
NM_002087.3:c.1403A>G
|
NP_002078.1:p.Gln468Arg
|
|
XM_005257253.1:c.1403A>G
|
XP_005257310.1:p.Gln468Arg
|
|
XM_024450730.1:c.1403A>G
|
XP_024306498.1:p.Gln468Arg
|
|
NM_002087.4:c.1403A>G
MANE Select
|
NP_002078.1:p.Gln468Arg
|
|