ENST00000683572.1:n.746C>T
|
|
|
ENST00000341947.7:c.4940C>T
MANE Select
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ENSP00000339915.2:p.Ala1647Val
|
|
ENST00000341947.6:c.4940C>T
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ENSP00000339915.2:p.Ala1647Val
|
|
ENST00000361917.5:c.4619C>T
|
ENSP00000355123.1:p.Ala1540Val
|
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ENST00000374708.8:c.4682C>T
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ENSP00000363840.4:p.Ala1561Val
|
|
ENST00000477772.1:n.730C>T
|
|
|
NM_080679.2:c.4619C>T
|
NP_542410.2:p.Ala1540Val
|
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NM_080680.2:c.4940C>T
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NP_542411.2:p.Ala1647Val
|
|
NM_080681.2:c.4682C>T
|
NP_542412.2:p.Ala1561Val
|
|
XM_011514298.1:c.4094C>T
|
XP_011512600.1:p.Ala1365Val
|
|
XM_011514299.1:c.4226C>T
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XP_011512601.1:p.Ala1409Val
|
|
XM_011514300.1:c.4046C>T
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XP_011512602.1:p.Ala1349Val
|
|
XM_011514301.1:c.3983C>T
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XP_011512603.1:p.Ala1328Val
|
|
XM_011514302.1:c.3827C>T
|
XP_011512604.1:p.Ala1276Val
|
|
XM_011514299.2:c.4226C>T
|
XP_011512601.1:p.Ala1409Val
|
|
XM_011514300.2:c.4046C>T
|
XP_011512602.1:p.Ala1349Val
|
|
XM_011514302.2:c.3827C>T
|
XP_011512604.1:p.Ala1276Val
|
|
XM_017010250.1:c.4940C>T
|
XP_016865739.1:p.Ala1647Val
|
|
XM_017010251.2:c.3758C>T
|
XP_016865740.1:p.Ala1253Val
|
|
NM_080680.3:c.4940C>T
MANE Select
|
NP_542411.2:p.Ala1647Val
|
|
NM_080681.3:c.4682C>T
|
NP_542412.2:p.Ala1561Val
|
|
NM_080679.3:c.4619C>T
|
NP_542410.2:p.Ala1540Val
|
|