ENST00000683572.1:n.564C>T
|
|
|
ENST00000341947.7:c.4758C>T
MANE Select
|
ENSP00000339915.2:p.Tyr1586=
|
|
ENST00000341947.6:c.4758C>T
|
ENSP00000339915.2:p.Tyr1586=
|
|
ENST00000361917.5:c.4437C>T
|
ENSP00000355123.1:p.Tyr1479=
|
|
ENST00000374708.8:c.4500C>T
|
ENSP00000363840.4:p.Tyr1500=
|
|
ENST00000477772.1:n.548C>T
|
|
|
NM_080679.2:c.4437C>T
|
NP_542410.2:p.Tyr1479=
|
|
NM_080680.2:c.4758C>T
|
NP_542411.2:p.Tyr1586=
|
|
NM_080681.2:c.4500C>T
|
NP_542412.2:p.Tyr1500=
|
|
XM_011514298.1:c.3912C>T
|
XP_011512600.1:p.Tyr1304=
|
|
XM_011514299.1:c.4044C>T
|
XP_011512601.1:p.Tyr1348=
|
|
XM_011514300.1:c.3864C>T
|
XP_011512602.1:p.Tyr1288=
|
|
XM_011514301.1:c.3801C>T
|
XP_011512603.1:p.Tyr1267=
|
|
XM_011514302.1:c.3645C>T
|
XP_011512604.1:p.Tyr1215=
|
|
XM_011514299.2:c.4044C>T
|
XP_011512601.1:p.Tyr1348=
|
|
XM_011514300.2:c.3864C>T
|
XP_011512602.1:p.Tyr1288=
|
|
XM_011514302.2:c.3645C>T
|
XP_011512604.1:p.Tyr1215=
|
|
XM_017010250.1:c.4758C>T
|
XP_016865739.1:p.Tyr1586=
|
|
XM_017010251.2:c.3576C>T
|
XP_016865740.1:p.Tyr1192=
|
|
NM_080680.3:c.4758C>T
MANE Select
|
NP_542411.2:p.Tyr1586=
|
|
NM_080681.3:c.4500C>T
|
NP_542412.2:p.Tyr1500=
|
|
NM_080679.3:c.4437C>T
|
NP_542410.2:p.Tyr1479=
|
|