ENST00000683572.1:n.746C>G
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ENST00000341947.7:c.4940C>G
MANE Select
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ENSP00000339915.2:p.Ala1647Gly
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ENST00000341947.6:c.4940C>G
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ENSP00000339915.2:p.Ala1647Gly
|
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ENST00000361917.5:c.4619C>G
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ENSP00000355123.1:p.Ala1540Gly
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ENST00000374708.8:c.4682C>G
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ENSP00000363840.4:p.Ala1561Gly
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ENST00000477772.1:n.730C>G
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NM_080679.2:c.4619C>G
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NP_542410.2:p.Ala1540Gly
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NM_080680.2:c.4940C>G
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NP_542411.2:p.Ala1647Gly
|
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NM_080681.2:c.4682C>G
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NP_542412.2:p.Ala1561Gly
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XM_011514298.1:c.4094C>G
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XP_011512600.1:p.Ala1365Gly
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XM_011514299.1:c.4226C>G
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XP_011512601.1:p.Ala1409Gly
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XM_011514300.1:c.4046C>G
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XP_011512602.1:p.Ala1349Gly
|
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XM_011514301.1:c.3983C>G
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XP_011512603.1:p.Ala1328Gly
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XM_011514302.1:c.3827C>G
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XP_011512604.1:p.Ala1276Gly
|
|
XM_011514299.2:c.4226C>G
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XP_011512601.1:p.Ala1409Gly
|
|
XM_011514300.2:c.4046C>G
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XP_011512602.1:p.Ala1349Gly
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XM_011514302.2:c.3827C>G
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XP_011512604.1:p.Ala1276Gly
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XM_017010250.1:c.4940C>G
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XP_016865739.1:p.Ala1647Gly
|
|
XM_017010251.2:c.3758C>G
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XP_016865740.1:p.Ala1253Gly
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NM_080680.3:c.4940C>G
MANE Select
|
NP_542411.2:p.Ala1647Gly
|
|
NM_080681.3:c.4682C>G
|
NP_542412.2:p.Ala1561Gly
|
|
NM_080679.3:c.4619C>G
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NP_542410.2:p.Ala1540Gly
|
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