ENST00000683572.1:n.778G>T
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ENST00000341947.7:c.4972G>T
MANE Select
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ENSP00000339915.2:p.Ala1658Ser
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ENST00000341947.6:c.4972G>T
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ENSP00000339915.2:p.Ala1658Ser
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ENST00000361917.5:c.4651G>T
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ENSP00000355123.1:p.Ala1551Ser
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ENST00000374708.8:c.4714G>T
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ENSP00000363840.4:p.Ala1572Ser
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ENST00000477772.1:n.762G>T
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NM_080679.2:c.4651G>T
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NP_542410.2:p.Ala1551Ser
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NM_080680.2:c.4972G>T
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NP_542411.2:p.Ala1658Ser
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NM_080681.2:c.4714G>T
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NP_542412.2:p.Ala1572Ser
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XM_011514298.1:c.4126G>T
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XP_011512600.1:p.Ala1376Ser
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XM_011514299.1:c.4258G>T
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XP_011512601.1:p.Ala1420Ser
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XM_011514300.1:c.4078G>T
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XP_011512602.1:p.Ala1360Ser
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XM_011514301.1:c.4015G>T
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XP_011512603.1:p.Ala1339Ser
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XM_011514302.1:c.3859G>T
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XP_011512604.1:p.Ala1287Ser
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XM_011514299.2:c.4258G>T
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XP_011512601.1:p.Ala1420Ser
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XM_011514300.2:c.4078G>T
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XP_011512602.1:p.Ala1360Ser
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XM_011514302.2:c.3859G>T
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XP_011512604.1:p.Ala1287Ser
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XM_017010250.1:c.4972G>T
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XP_016865739.1:p.Ala1658Ser
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XM_017010251.2:c.3790G>T
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XP_016865740.1:p.Ala1264Ser
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NM_080680.3:c.4972G>T
MANE Select
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NP_542411.2:p.Ala1658Ser
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NM_080681.3:c.4714G>T
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NP_542412.2:p.Ala1572Ser
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NM_080679.3:c.4651G>T
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NP_542410.2:p.Ala1551Ser
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