ENST00000683572.1:n.616A>T
|
|
|
ENST00000341947.7:c.4810A>T
MANE Select
|
ENSP00000339915.2:p.Asn1604Tyr
|
|
ENST00000341947.6:c.4810A>T
|
ENSP00000339915.2:p.Asn1604Tyr
|
|
ENST00000361917.5:c.4489A>T
|
ENSP00000355123.1:p.Asn1497Tyr
|
|
ENST00000374708.8:c.4552A>T
|
ENSP00000363840.4:p.Asn1518Tyr
|
|
ENST00000477772.1:n.600A>T
|
|
|
NM_080679.2:c.4489A>T
|
NP_542410.2:p.Asn1497Tyr
|
|
NM_080680.2:c.4810A>T
|
NP_542411.2:p.Asn1604Tyr
|
|
NM_080681.2:c.4552A>T
|
NP_542412.2:p.Asn1518Tyr
|
|
XM_011514298.1:c.3964A>T
|
XP_011512600.1:p.Asn1322Tyr
|
|
XM_011514299.1:c.4096A>T
|
XP_011512601.1:p.Asn1366Tyr
|
|
XM_011514300.1:c.3916A>T
|
XP_011512602.1:p.Asn1306Tyr
|
|
XM_011514301.1:c.3853A>T
|
XP_011512603.1:p.Asn1285Tyr
|
|
XM_011514302.1:c.3697A>T
|
XP_011512604.1:p.Asn1233Tyr
|
|
XM_011514299.2:c.4096A>T
|
XP_011512601.1:p.Asn1366Tyr
|
|
XM_011514300.2:c.3916A>T
|
XP_011512602.1:p.Asn1306Tyr
|
|
XM_011514302.2:c.3697A>T
|
XP_011512604.1:p.Asn1233Tyr
|
|
XM_017010250.1:c.4810A>T
|
XP_016865739.1:p.Asn1604Tyr
|
|
XM_017010251.2:c.3628A>T
|
XP_016865740.1:p.Asn1210Tyr
|
|
NM_080680.3:c.4810A>T
MANE Select
|
NP_542411.2:p.Asn1604Tyr
|
|
NM_080681.3:c.4552A>T
|
NP_542412.2:p.Asn1518Tyr
|
|
NM_080679.3:c.4489A>T
|
NP_542410.2:p.Asn1497Tyr
|
|