ENST00000683572.1:n.788A=
|
|
|
ENST00000341947.7:c.4982A=
MANE Select
|
ENSP00000339915.2:p.Asp1661=
|
|
ENST00000341947.6:c.4982A=
|
ENSP00000339915.2:p.Asp1661=
|
|
ENST00000361917.5:c.4661A=
|
ENSP00000355123.1:p.Asp1554=
|
|
ENST00000374708.8:c.4724A=
|
ENSP00000363840.4:p.Asp1575=
|
|
ENST00000477772.1:n.772A=
|
|
|
NM_080679.2:c.4661A=
|
NP_542410.2:p.Asp1554=
|
|
NM_080680.2:c.4982A=
|
NP_542411.2:p.Asp1661=
|
|
NM_080681.2:c.4724A=
|
NP_542412.2:p.Asp1575=
|
|
XM_011514298.1:c.4136A=
|
XP_011512600.1:p.Asp1379=
|
|
XM_011514299.1:c.4268A=
|
XP_011512601.1:p.Asp1423=
|
|
XM_011514300.1:c.4088A=
|
XP_011512602.1:p.Asp1363=
|
|
XM_011514301.1:c.4025A=
|
XP_011512603.1:p.Asp1342=
|
|
XM_011514302.1:c.3869A=
|
XP_011512604.1:p.Asp1290=
|
|
XM_011514299.2:c.4268A=
|
XP_011512601.1:p.Asp1423=
|
|
XM_011514300.2:c.4088A=
|
XP_011512602.1:p.Asp1363=
|
|
XM_011514302.2:c.3869A=
|
XP_011512604.1:p.Asp1290=
|
|
XM_017010250.1:c.4982A=
|
XP_016865739.1:p.Asp1661=
|
|
XM_017010251.2:c.3800A=
|
XP_016865740.1:p.Asp1267=
|
|
NM_080680.3:c.4982A=
MANE Select
|
NP_542411.2:p.Asp1661=
|
|
NM_080681.3:c.4724A=
|
NP_542412.2:p.Asp1575=
|
|
NM_080679.3:c.4661A=
|
NP_542410.2:p.Asp1554=
|
|