ENST00000683572.1:n.751C>G
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|
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ENST00000341947.7:c.4945C>G
MANE Select
|
ENSP00000339915.2:p.Gln1649Glu
|
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ENST00000341947.6:c.4945C>G
|
ENSP00000339915.2:p.Gln1649Glu
|
|
ENST00000361917.5:c.4624C>G
|
ENSP00000355123.1:p.Gln1542Glu
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ENST00000374708.8:c.4687C>G
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ENSP00000363840.4:p.Gln1563Glu
|
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ENST00000477772.1:n.735C>G
|
|
|
NM_080679.2:c.4624C>G
|
NP_542410.2:p.Gln1542Glu
|
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NM_080680.2:c.4945C>G
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NP_542411.2:p.Gln1649Glu
|
|
NM_080681.2:c.4687C>G
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NP_542412.2:p.Gln1563Glu
|
|
XM_011514298.1:c.4099C>G
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XP_011512600.1:p.Gln1367Glu
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XM_011514299.1:c.4231C>G
|
XP_011512601.1:p.Gln1411Glu
|
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XM_011514300.1:c.4051C>G
|
XP_011512602.1:p.Gln1351Glu
|
|
XM_011514301.1:c.3988C>G
|
XP_011512603.1:p.Gln1330Glu
|
|
XM_011514302.1:c.3832C>G
|
XP_011512604.1:p.Gln1278Glu
|
|
XM_011514299.2:c.4231C>G
|
XP_011512601.1:p.Gln1411Glu
|
|
XM_011514300.2:c.4051C>G
|
XP_011512602.1:p.Gln1351Glu
|
|
XM_011514302.2:c.3832C>G
|
XP_011512604.1:p.Gln1278Glu
|
|
XM_017010250.1:c.4945C>G
|
XP_016865739.1:p.Gln1649Glu
|
|
XM_017010251.2:c.3763C>G
|
XP_016865740.1:p.Gln1255Glu
|
|
NM_080680.3:c.4945C>G
MANE Select
|
NP_542411.2:p.Gln1649Glu
|
|
NM_080681.3:c.4687C>G
|
NP_542412.2:p.Gln1563Glu
|
|
NM_080679.3:c.4624C>G
|
NP_542410.2:p.Gln1542Glu
|
|