ENST00000683572.1:n.704G>T
|
|
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ENST00000341947.7:c.4898G>T
MANE Select
|
ENSP00000339915.2:p.Gly1633Val
|
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ENST00000341947.6:c.4898G>T
|
ENSP00000339915.2:p.Gly1633Val
|
|
ENST00000361917.5:c.4577G>T
|
ENSP00000355123.1:p.Gly1526Val
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ENST00000374708.8:c.4640G>T
|
ENSP00000363840.4:p.Gly1547Val
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ENST00000477772.1:n.688G>T
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|
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NM_080679.2:c.4577G>T
|
NP_542410.2:p.Gly1526Val
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|
NM_080680.2:c.4898G>T
|
NP_542411.2:p.Gly1633Val
|
|
NM_080681.2:c.4640G>T
|
NP_542412.2:p.Gly1547Val
|
|
XM_011514298.1:c.4052G>T
|
XP_011512600.1:p.Gly1351Val
|
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XM_011514299.1:c.4184G>T
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XP_011512601.1:p.Gly1395Val
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|
XM_011514300.1:c.4004G>T
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XP_011512602.1:p.Gly1335Val
|
|
XM_011514301.1:c.3941G>T
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XP_011512603.1:p.Gly1314Val
|
|
XM_011514302.1:c.3785G>T
|
XP_011512604.1:p.Gly1262Val
|
|
XM_011514299.2:c.4184G>T
|
XP_011512601.1:p.Gly1395Val
|
|
XM_011514300.2:c.4004G>T
|
XP_011512602.1:p.Gly1335Val
|
|
XM_011514302.2:c.3785G>T
|
XP_011512604.1:p.Gly1262Val
|
|
XM_017010250.1:c.4898G>T
|
XP_016865739.1:p.Gly1633Val
|
|
XM_017010251.2:c.3716G>T
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XP_016865740.1:p.Gly1239Val
|
|
NM_080680.3:c.4898G>T
MANE Select
|
NP_542411.2:p.Gly1633Val
|
|
NM_080681.3:c.4640G>T
|
NP_542412.2:p.Gly1547Val
|
|
NM_080679.3:c.4577G>T
|
NP_542410.2:p.Gly1526Val
|
|