ENST00000231749.8:c.575G=
MANE Select
|
ENSP00000231749.3:p.Arg192=
|
|
ENST00000231749.7:c.575G=
|
ENSP00000231749.3:p.Arg192=
|
|
ENST00000360165.7:c.575G=
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ENSP00000353289.3:p.Arg192=
|
|
ENST00000442887.1:c.446G=
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ENSP00000393687.1:p.Arg149=
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|
ENST00000443080.5:c.*327G=
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ENSP00000415661.1:n.*327G=
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|
ENST00000475688.1:n.27G=
|
|
|
NM_001308379.1:c.575G=
|
NP_001295308.1:p.Arg192=
|
|
NM_015896.2:c.575G=
|
NP_056980.2:p.Arg192=
|
|
NM_015896.3:c.575G=
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NP_056980.2:p.Arg192=
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|
XM_005265216.2:c.338G=
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XP_005265273.1:p.Arg113=
|
|
XM_005265216.3:c.338G=
|
XP_005265273.1:p.Arg113=
|
|
NM_015896.4:c.575G=
MANE Select
|
NP_056980.2:p.Arg192=
|
|
NM_001308379.2:c.575G=
|
NP_001295308.1:p.Arg192=
|
|