ENST00000683572.1:n.562T>A
|
|
|
ENST00000341947.7:c.4756T>A
MANE Select
|
ENSP00000339915.2:p.Tyr1586Asn
|
|
ENST00000341947.6:c.4756T>A
|
ENSP00000339915.2:p.Tyr1586Asn
|
|
ENST00000361917.5:c.4435T>A
|
ENSP00000355123.1:p.Tyr1479Asn
|
|
ENST00000374708.8:c.4498T>A
|
ENSP00000363840.4:p.Tyr1500Asn
|
|
ENST00000477772.1:n.546T>A
|
|
|
NM_080679.2:c.4435T>A
|
NP_542410.2:p.Tyr1479Asn
|
|
NM_080680.2:c.4756T>A
|
NP_542411.2:p.Tyr1586Asn
|
|
NM_080681.2:c.4498T>A
|
NP_542412.2:p.Tyr1500Asn
|
|
XM_011514298.1:c.3910T>A
|
XP_011512600.1:p.Tyr1304Asn
|
|
XM_011514299.1:c.4042T>A
|
XP_011512601.1:p.Tyr1348Asn
|
|
XM_011514300.1:c.3862T>A
|
XP_011512602.1:p.Tyr1288Asn
|
|
XM_011514301.1:c.3799T>A
|
XP_011512603.1:p.Tyr1267Asn
|
|
XM_011514302.1:c.3643T>A
|
XP_011512604.1:p.Tyr1215Asn
|
|
XM_011514299.2:c.4042T>A
|
XP_011512601.1:p.Tyr1348Asn
|
|
XM_011514300.2:c.3862T>A
|
XP_011512602.1:p.Tyr1288Asn
|
|
XM_011514302.2:c.3643T>A
|
XP_011512604.1:p.Tyr1215Asn
|
|
XM_017010250.1:c.4756T>A
|
XP_016865739.1:p.Tyr1586Asn
|
|
XM_017010251.2:c.3574T>A
|
XP_016865740.1:p.Tyr1192Asn
|
|
NM_080680.3:c.4756T>A
MANE Select
|
NP_542411.2:p.Tyr1586Asn
|
|
NM_080681.3:c.4498T>A
|
NP_542412.2:p.Tyr1500Asn
|
|
NM_080679.3:c.4435T>A
|
NP_542410.2:p.Tyr1479Asn
|
|