ENST00000683572.1:n.776G>T
|
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ENST00000341947.7:c.4970G>T
MANE Select
|
ENSP00000339915.2:p.Gly1657Val
|
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ENST00000341947.6:c.4970G>T
|
ENSP00000339915.2:p.Gly1657Val
|
|
ENST00000361917.5:c.4649G>T
|
ENSP00000355123.1:p.Gly1550Val
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ENST00000374708.8:c.4712G>T
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ENSP00000363840.4:p.Gly1571Val
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ENST00000477772.1:n.760G>T
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|
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NM_080679.2:c.4649G>T
|
NP_542410.2:p.Gly1550Val
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|
NM_080680.2:c.4970G>T
|
NP_542411.2:p.Gly1657Val
|
|
NM_080681.2:c.4712G>T
|
NP_542412.2:p.Gly1571Val
|
|
XM_011514298.1:c.4124G>T
|
XP_011512600.1:p.Gly1375Val
|
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XM_011514299.1:c.4256G>T
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XP_011512601.1:p.Gly1419Val
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XM_011514300.1:c.4076G>T
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XP_011512602.1:p.Gly1359Val
|
|
XM_011514301.1:c.4013G>T
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XP_011512603.1:p.Gly1338Val
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XM_011514302.1:c.3857G>T
|
XP_011512604.1:p.Gly1286Val
|
|
XM_011514299.2:c.4256G>T
|
XP_011512601.1:p.Gly1419Val
|
|
XM_011514300.2:c.4076G>T
|
XP_011512602.1:p.Gly1359Val
|
|
XM_011514302.2:c.3857G>T
|
XP_011512604.1:p.Gly1286Val
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XM_017010250.1:c.4970G>T
|
XP_016865739.1:p.Gly1657Val
|
|
XM_017010251.2:c.3788G>T
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XP_016865740.1:p.Gly1263Val
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|
NM_080680.3:c.4970G>T
MANE Select
|
NP_542411.2:p.Gly1657Val
|
|
NM_080681.3:c.4712G>T
|
NP_542412.2:p.Gly1571Val
|
|
NM_080679.3:c.4649G>T
|
NP_542410.2:p.Gly1550Val
|
|