ENST00000683572.1:n.719C=
|
|
|
ENST00000341947.7:c.4913C=
MANE Select
|
ENSP00000339915.2:p.Thr1638=
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ENST00000341947.6:c.4913C=
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ENSP00000339915.2:p.Thr1638=
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|
ENST00000361917.5:c.4592C=
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ENSP00000355123.1:p.Thr1531=
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ENST00000374708.8:c.4655C=
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ENSP00000363840.4:p.Thr1552=
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|
ENST00000477772.1:n.703C=
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|
|
NM_080679.2:c.4592C=
|
NP_542410.2:p.Thr1531=
|
|
NM_080680.2:c.4913C=
|
NP_542411.2:p.Thr1638=
|
|
NM_080681.2:c.4655C=
|
NP_542412.2:p.Thr1552=
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|
XM_011514298.1:c.4067C=
|
XP_011512600.1:p.Thr1356=
|
|
XM_011514299.1:c.4199C=
|
XP_011512601.1:p.Thr1400=
|
|
XM_011514300.1:c.4019C=
|
XP_011512602.1:p.Thr1340=
|
|
XM_011514301.1:c.3956C=
|
XP_011512603.1:p.Thr1319=
|
|
XM_011514302.1:c.3800C=
|
XP_011512604.1:p.Thr1267=
|
|
XM_011514299.2:c.4199C=
|
XP_011512601.1:p.Thr1400=
|
|
XM_011514300.2:c.4019C=
|
XP_011512602.1:p.Thr1340=
|
|
XM_011514302.2:c.3800C=
|
XP_011512604.1:p.Thr1267=
|
|
XM_017010250.1:c.4913C=
|
XP_016865739.1:p.Thr1638=
|
|
XM_017010251.2:c.3731C=
|
XP_016865740.1:p.Thr1244=
|
|
NM_080680.3:c.4913C=
MANE Select
|
NP_542411.2:p.Thr1638=
|
|
NM_080681.3:c.4655C=
|
NP_542412.2:p.Thr1552=
|
|
NM_080679.3:c.4592C=
|
NP_542410.2:p.Thr1531=
|
|