ENST00000683572.1:n.736A=
|
|
|
ENST00000341947.7:c.4930A=
MANE Select
|
ENSP00000339915.2:p.Ser1644=
|
|
ENST00000341947.6:c.4930A=
|
ENSP00000339915.2:p.Ser1644=
|
|
ENST00000361917.5:c.4609A=
|
ENSP00000355123.1:p.Ser1537=
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|
ENST00000374708.8:c.4672A=
|
ENSP00000363840.4:p.Ser1558=
|
|
ENST00000477772.1:n.720A=
|
|
|
NM_080679.2:c.4609A=
|
NP_542410.2:p.Ser1537=
|
|
NM_080680.2:c.4930A=
|
NP_542411.2:p.Ser1644=
|
|
NM_080681.2:c.4672A=
|
NP_542412.2:p.Ser1558=
|
|
XM_011514298.1:c.4084A=
|
XP_011512600.1:p.Ser1362=
|
|
XM_011514299.1:c.4216A=
|
XP_011512601.1:p.Ser1406=
|
|
XM_011514300.1:c.4036A=
|
XP_011512602.1:p.Ser1346=
|
|
XM_011514301.1:c.3973A=
|
XP_011512603.1:p.Ser1325=
|
|
XM_011514302.1:c.3817A=
|
XP_011512604.1:p.Ser1273=
|
|
XM_011514299.2:c.4216A=
|
XP_011512601.1:p.Ser1406=
|
|
XM_011514300.2:c.4036A=
|
XP_011512602.1:p.Ser1346=
|
|
XM_011514302.2:c.3817A=
|
XP_011512604.1:p.Ser1273=
|
|
XM_017010250.1:c.4930A=
|
XP_016865739.1:p.Ser1644=
|
|
XM_017010251.2:c.3748A=
|
XP_016865740.1:p.Ser1250=
|
|
NM_080680.3:c.4930A=
MANE Select
|
NP_542411.2:p.Ser1644=
|
|
NM_080681.3:c.4672A=
|
NP_542412.2:p.Ser1558=
|
|
NM_080679.3:c.4609A=
|
NP_542410.2:p.Ser1537=
|
|