ENST00000683572.1:n.799A>T
|
|
|
ENST00000341947.7:c.4993A>T
MANE Select
|
ENSP00000339915.2:p.Arg1665Ter
|
|
ENST00000341947.6:c.4993A>T
|
ENSP00000339915.2:p.Arg1665Ter
|
|
ENST00000361917.5:c.4672A>T
|
ENSP00000355123.1:p.Arg1558Ter
|
|
ENST00000374708.8:c.4735A>T
|
ENSP00000363840.4:p.Arg1579Ter
|
|
ENST00000477772.1:n.783A>T
|
|
|
NM_080679.2:c.4672A>T
|
NP_542410.2:p.Arg1558Ter
|
|
NM_080680.2:c.4993A>T
|
NP_542411.2:p.Arg1665Ter
|
|
NM_080681.2:c.4735A>T
|
NP_542412.2:p.Arg1579Ter
|
|
XM_011514298.1:c.4147A>T
|
XP_011512600.1:p.Arg1383Ter
|
|
XM_011514299.1:c.4279A>T
|
XP_011512601.1:p.Arg1427Ter
|
|
XM_011514300.1:c.4099A>T
|
XP_011512602.1:p.Arg1367Ter
|
|
XM_011514301.1:c.4036A>T
|
XP_011512603.1:p.Arg1346Ter
|
|
XM_011514302.1:c.3880A>T
|
XP_011512604.1:p.Arg1294Ter
|
|
XM_011514299.2:c.4279A>T
|
XP_011512601.1:p.Arg1427Ter
|
|
XM_011514300.2:c.4099A>T
|
XP_011512602.1:p.Arg1367Ter
|
|
XM_011514302.2:c.3880A>T
|
XP_011512604.1:p.Arg1294Ter
|
|
XM_017010250.1:c.4993A>T
|
XP_016865739.1:p.Arg1665Ter
|
|
XM_017010251.2:c.3811A>T
|
XP_016865740.1:p.Arg1271Ter
|
|
NM_080680.3:c.4993A>T
MANE Select
|
NP_542411.2:p.Arg1665Ter
|
|
NM_080681.3:c.4735A>T
|
NP_542412.2:p.Arg1579Ter
|
|
NM_080679.3:c.4672A>T
|
NP_542410.2:p.Arg1558Ter
|
|