ENST00000341947.7:c.3718G>A
MANE Select
|
ENSP00000339915.2:p.Gly1240Arg
|
|
ENST00000341947.6:c.3718G>A
|
ENSP00000339915.2:p.Gly1240Arg
|
|
ENST00000361917.5:c.3397G>A
|
ENSP00000355123.1:p.Gly1133Arg
|
|
ENST00000374708.8:c.3460G>A
|
ENSP00000363840.4:p.Gly1154Arg
|
|
ENST00000477772.1:n.273-3647G>A
|
|
|
NM_080679.2:c.3397G>A
|
NP_542410.2:p.Gly1133Arg
|
|
NM_080680.2:c.3718G>A
|
NP_542411.2:p.Gly1240Arg
|
|
NM_080681.2:c.3460G>A
|
NP_542412.2:p.Gly1154Arg
|
|
XM_011514298.1:c.2872G>A
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XP_011512600.1:p.Gly958Arg
|
|
XM_011514299.1:c.3004G>A
|
XP_011512601.1:p.Gly1002Arg
|
|
XM_011514300.1:c.2824G>A
|
XP_011512602.1:p.Gly942Arg
|
|
XM_011514301.1:c.2761G>A
|
XP_011512603.1:p.Gly921Arg
|
|
XM_011514302.1:c.2605G>A
|
XP_011512604.1:p.Gly869Arg
|
|
XM_011514299.2:c.3004G>A
|
XP_011512601.1:p.Gly1002Arg
|
|
XM_011514300.2:c.2824G>A
|
XP_011512602.1:p.Gly942Arg
|
|
XM_011514302.2:c.2605G>A
|
XP_011512604.1:p.Gly869Arg
|
|
XM_017010250.1:c.3718G>A
|
XP_016865739.1:p.Gly1240Arg
|
|
XM_017010251.2:c.2536G>A
|
XP_016865740.1:p.Gly846Arg
|
|
NM_080680.3:c.3718G>A
MANE Select
|
NP_542411.2:p.Gly1240Arg
|
|
NM_080681.3:c.3460G>A
|
NP_542412.2:p.Gly1154Arg
|
|
NM_080679.3:c.3397G>A
|
NP_542410.2:p.Gly1133Arg
|
|