ENST00000683572.1:n.764A>C
|
|
|
ENST00000341947.7:c.4958A>C
MANE Select
|
ENSP00000339915.2:p.Tyr1653Ser
|
|
ENST00000341947.6:c.4958A>C
|
ENSP00000339915.2:p.Tyr1653Ser
|
|
ENST00000361917.5:c.4637A>C
|
ENSP00000355123.1:p.Tyr1546Ser
|
|
ENST00000374708.8:c.4700A>C
|
ENSP00000363840.4:p.Tyr1567Ser
|
|
ENST00000477772.1:n.748A>C
|
|
|
NM_080679.2:c.4637A>C
|
NP_542410.2:p.Tyr1546Ser
|
|
NM_080680.2:c.4958A>C
|
NP_542411.2:p.Tyr1653Ser
|
|
NM_080681.2:c.4700A>C
|
NP_542412.2:p.Tyr1567Ser
|
|
XM_011514298.1:c.4112A>C
|
XP_011512600.1:p.Tyr1371Ser
|
|
XM_011514299.1:c.4244A>C
|
XP_011512601.1:p.Tyr1415Ser
|
|
XM_011514300.1:c.4064A>C
|
XP_011512602.1:p.Tyr1355Ser
|
|
XM_011514301.1:c.4001A>C
|
XP_011512603.1:p.Tyr1334Ser
|
|
XM_011514302.1:c.3845A>C
|
XP_011512604.1:p.Tyr1282Ser
|
|
XM_011514299.2:c.4244A>C
|
XP_011512601.1:p.Tyr1415Ser
|
|
XM_011514300.2:c.4064A>C
|
XP_011512602.1:p.Tyr1355Ser
|
|
XM_011514302.2:c.3845A>C
|
XP_011512604.1:p.Tyr1282Ser
|
|
XM_017010250.1:c.4958A>C
|
XP_016865739.1:p.Tyr1653Ser
|
|
XM_017010251.2:c.3776A>C
|
XP_016865740.1:p.Tyr1259Ser
|
|
NM_080680.3:c.4958A>C
MANE Select
|
NP_542411.2:p.Tyr1653Ser
|
|
NM_080681.3:c.4700A>C
|
NP_542412.2:p.Tyr1567Ser
|
|
NM_080679.3:c.4637A>C
|
NP_542410.2:p.Tyr1546Ser
|
|