ENST00000053867.8:c.1399T>C
MANE Select
|
ENSP00000053867.2:p.Cys467Arg
|
|
ENST00000639447.1:c.1137-295T>C
|
ENSP00000492014.1:n.1137-295T>C
|
|
ENST00000053867.7:c.1399T>C
|
ENSP00000053867.2:p.Cys467Arg
|
|
ENST00000586242.1:c.33T>C
|
|
|
ENST00000586443.1:c.840T>C
|
|
|
ENST00000589265.5:c.928T>C
|
ENSP00000467616.1:p.Cys310Arg
|
|
NM_002087.3:c.1399T>C
|
NP_002078.1:p.Cys467Arg
|
|
XM_005257253.1:c.1399T>C
|
XP_005257310.1:p.Cys467Arg
|
|
XM_024450730.1:c.1399T>C
|
XP_024306498.1:p.Cys467Arg
|
|
NM_002087.4:c.1399T>C
MANE Select
|
NP_002078.1:p.Cys467Arg
|
|