ENST00000683572.1:n.790G>C
|
|
|
ENST00000341947.7:c.4984G>C
MANE Select
|
ENSP00000339915.2:p.Gly1662Arg
|
|
ENST00000341947.6:c.4984G>C
|
ENSP00000339915.2:p.Gly1662Arg
|
|
ENST00000361917.5:c.4663G>C
|
ENSP00000355123.1:p.Gly1555Arg
|
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ENST00000374708.8:c.4726G>C
|
ENSP00000363840.4:p.Gly1576Arg
|
|
ENST00000477772.1:n.774G>C
|
|
|
NM_080679.2:c.4663G>C
|
NP_542410.2:p.Gly1555Arg
|
|
NM_080680.2:c.4984G>C
|
NP_542411.2:p.Gly1662Arg
|
|
NM_080681.2:c.4726G>C
|
NP_542412.2:p.Gly1576Arg
|
|
XM_011514298.1:c.4138G>C
|
XP_011512600.1:p.Gly1380Arg
|
|
XM_011514299.1:c.4270G>C
|
XP_011512601.1:p.Gly1424Arg
|
|
XM_011514300.1:c.4090G>C
|
XP_011512602.1:p.Gly1364Arg
|
|
XM_011514301.1:c.4027G>C
|
XP_011512603.1:p.Gly1343Arg
|
|
XM_011514302.1:c.3871G>C
|
XP_011512604.1:p.Gly1291Arg
|
|
XM_011514299.2:c.4270G>C
|
XP_011512601.1:p.Gly1424Arg
|
|
XM_011514300.2:c.4090G>C
|
XP_011512602.1:p.Gly1364Arg
|
|
XM_011514302.2:c.3871G>C
|
XP_011512604.1:p.Gly1291Arg
|
|
XM_017010250.1:c.4984G>C
|
XP_016865739.1:p.Gly1662Arg
|
|
XM_017010251.2:c.3802G>C
|
XP_016865740.1:p.Gly1268Arg
|
|
NM_080680.3:c.4984G>C
MANE Select
|
NP_542411.2:p.Gly1662Arg
|
|
NM_080681.3:c.4726G>C
|
NP_542412.2:p.Gly1576Arg
|
|
NM_080679.3:c.4663G>C
|
NP_542410.2:p.Gly1555Arg
|
|